Rorgamma modulators and uses thereof

ABSTRACT

The present invention provides novel compounds of formula (Ia) that are modulators of RORgamma. These compounds, and pharmaceutical compositions comprising the same, are suitable means for treating any disease wherein the modulation of RORgamma has therapeutic effects, for instance in autoimmune diseases, autoimmune-related diseases, inflammatory diseases, metabolic diseases, fibrotic diseases, or cholestatic diseases.

TECHNICAL FIELD

The present invention relates to novel compounds that are modulators of RORgamma and the pharmaceutical use of such compounds.

BACKGROUND

The retinoic acid-related orphan receptor γ (RORγ) is a member of the ROR subfamily of nuclear receptors which includes three genes; RORA, RORB and RORC (also known as RORγ). rorγ gene encodes two isoforms RORγ1 and RORγ2 (also termed RORγt). RORγ1 is preferentially expressed in skeletal muscle and several other tissues, including pancreas, thymus, prostate, liver and testis (Hirose et al, 1994; Ortiz et al, 1995). RORγt is restricted to several distinct immune cell types (He et al, 1998). This immune system-specific isoform (RORγt) is the key lineage-defining transcription factor for the differentiation program of T helper type 17 (Th17) cells, a subset of CD4+T-helper and the most prominent cells in producing a number of inflammatory cytokines, such as IL-17A, IL-17F, IL-22, and IL-23 considered as important pathogenic factors for many immune and inflammatory diseases. During the disease process Th17 cells are activated and are responsible for recruiting other inflammatory cell types, such as neutrophils, to mediate pathology in the target tissues (Korn et al, 2009). RORγt is also able to induce IL-17A and IL-17F in naïve CD4+T-helper, NKT and iNKT cells (Rachitskaya et al, 2008), γδT cells (Murdoch & Lloyd, 2010), CD8+ Tcells (Liu et al, 2007) and CD4-CD8+TCRab+T cells (Crispin et al, 2008). RORγt is also expressed in and is required for the generation of LTi cells (Eberl et al, 2004), which are central to the development of lymphoid organs such as lymph node and Peyer's patch (Lipp & Muller, 2004).

Overexpression of RORγt in naïve CD4+ T cells was demonstrated to drive the induction and development of Th17 cells. In contrast, RORγt deficiency in mice completely impairs Th17 cell differentiation and induces resistance to the development of autoimmune diseases, such as experimental autoimmune encephalomyelitis (EAE) a model of multiple sclerosis (Dang et al, 2011; Yang et al, 2008) or experimental autoimmune myocarditis (EAM) (Yamashita et al, 2011). In the same manner, mice lacking IL-17 are resistant to development of EAE, and collagen-induced arthritis (CIA), a model of rheumatoid arthritis. IL-17 neutralization with a targeted antibody suppresses autoimmune inflammation, joint damage, and bone destruction (Furuzawa-Carballeda et al, 2007; Lubberts et al, 2004; Stockinger et al, 2007). Moreover, blocking Th17 pathway demonstrated good efficacy in patients with some chronic inflammatory diseases. For example, the anti-p40 monoclonal antibody Ustekinumab (Stelara) that targets Th17 and Th1 through IL-23 and IL-12 respectively, has been approved for the treatment of moderate to severe plaque psoriasis in adult patients and showed a clinical (phase IIb) efficacy in refractory Crohn diseased patients (Tuskey & Behm, 2014).

Small molecule RORγt modulators have therapeutic effects in preclinical disease models. In particular, compounds TMP778 and SR1001 were efficacious in psoriasis and multiple sclerosis models, respectively, when administered by injection (Skepner et al, 2014; Solt et al, 2011). Recently, Vitae Pharma has announced that a small molecule RORgt inverse agonist VTP-43742 reduced the Psoriasis Area Severity Index (PASI) score and plasma IL-17 levels, relative to placebo, in patients with moderate to severe psoriasis.

To summarise, RORγt activity modulation results in the modulation of IL-17 dependent immune and inflammatory responses.

Currently, there is considerable evidence suggesting that RORγt/IL-17 component is closely associated with a range of chronic inflammatory diseases such as multiple sclerosis (MS), psoriasis, inflammatory bowel diseases (IBD), rheumatoid arthritis (RA), uveitis and lung diseases. Compounds able to modulate RORγt activity are also expected to provide a therapeutic benefit in the treatment of numerous medical disorders, including autoimmune, inflammatory, fibrotic and cholestatic disorders, such as asthma, ankylosing spondylitis, autoimmune cardiomyopathy, autoimmune hepatitis, Crohn's disease, chronic obstructive proliferative disease (COPD), diabetes mellitus type 1, lupus erythematosus, lupus nephritis, multiple sclerosis, psoriasis, psoriatic arthritis, rheumatoid arthritis, ulcerative colitis, myocarditis, pulmonary fibrosis (idiopathic pulmonary, interstitial lung, cystic and progressive massive fibrosis), Non Alcoholic Fatty Liver Disease (NAFLD), NonAlcoholic SteatoHepatitis (NASH) and Alcoholic SteatoHepatitis (ASH), cardiac fibrosis and heart myocardial and endomyocardial fibrosis, arterial fibrosis, atherosclerosis/restenosis, intestinal fibrosis (occurs for example in Crohn's disease and collagenous colitis), kidney fibrosis, scleroderma and systemic sclerosis Primary Biliary Cholangitis (PBC), primary sclerosisng cholangitis (PSC), billiary artesia, Progressive familial intrahepatic cholestasis (PFIC), Hepatitis (hepatitis A, hepatitis B, hepatitis C).

The present invention describes novel RORγt modulators, their preparation and their use in therapy, in particular in the treatment of immune, inflammatory, metabolic, fibrotic and cholestatic diseases.

SUMMARY OF INVENTION

RORγ inverse agonists were proposed in Skepner et al., 2014 who allegedly showed that compound T was efficacious in psoriasis model when administered by injection.

Recently, data from a Phase 2a proof-of-concept clinical trial with RORgt inverse agonist (VTP-43742) were reported (Vitae Pharma press release). VTP-43742 demonstrated a clear signal of efficacy, with patients in the 350 mg dose group achieving a 24 percent reduction in the Psoriasis Area Severity Index (PASI) score relative to placebo. In the 700 mg dose group, patients achieved a 30 percent placebo-adjusted PASI score reduction.

The present invention thus provides novel compounds that are modulators of RORγ and have the following formula (I) or (Ia).

The present invention also provides pharmaceutical compositions comprising the compounds of formula (I) or (Ia) since they modulate RORγ in vitro and in cellular models, indicating that these compounds have properties of pharmaceutical interest. Accordingly, further objects of the invention include methods of treatment comprising the administration of said pharmaceutical composition for the treatment of RORγ-related diseases such as autoimmune, inflammatory diseases, metabolic, fibrotic and cholestatic diseases.

The present invention also provides a compound of formula (I) or (Ia), for use as a medicament.

The present invention also provides a compound of formula (I) or (Ia), for use in a method for the treatment of RORγ-related diseases.

Further objects of the present invention, including preferred compounds of formula (I) or (Ia), methods of preparing compounds of formula (I) or (Ia) and preferred medical uses or methods, in combination or not with other compounds, are provided in the Detailed Description.

DESCRIPTION OF THE FIGURES Abbreviations Used in the Figures and in the Text

-   -   ACLF acute-on-chronic liver failure     -   ADME absorption, distribution, metabolism, and excretion     -   ALF acute liver failure     -   ASH Alcoholic SteatoHepatitis     -   BINAP 2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene     -   CD Cluster of Differentiation     -   CDCl3 deuterated chloroform     -   CFA Complete Freund's Adjuvant     -   CH2Cl2 Dichloromethane     -   CH3CN acetonitrile     -   CIA collagen-induced arthritis     -   CMC CarboxyMethyl Cellulose     -   CNS Conserved non coding sequence     -   COPD chronic obstructive proliferative disease     -   Cpd: Compound     -   Cs2CO3 cesium carbonate     -   DavePhos 2-Dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl     -   DIPEA N,N-Diisopropylethylamine     -   DMAP 4-(DiMethylAmino)Pyridine     -   DMEM Dulbecco's modified Eagle's medium     -   DMF DiMethylFormamide     -   DMSO DiMethyl SulfOxide     -   eADME Early Absorption, Distribution, Metabolism, and Excretion     -   EAE experimental autoimmune encephalomyelitis     -   EAM Experimental Autoimmune Myocarditis     -   EDCl.HCl N-Ethyl-N′-(3-Dimethylaminopropyl)Carbodilmide         HydroChloride     -   equiv equivalent     -   Et2O Diethyl ether     -   EtOAc Ethyl acetate     -   H2O water     -   H2SO4 Sulfuric acid     -   HCl Hydrochloric acid     -   HPLC High Performance Liquid Chromatography     -   IBD Inflammatory Bowel Diseases     -   IC₅₀ Half maximal inhibitory concentration     -   ICP Intarhepatic Cholestasis of Pregnancy     -   IL-12 interleukin 12     -   IL-17 interleukin 17     -   IL-23 interleukin 23     -   IUPAC International Union of Pure and Applied Chemistry     -   K3PO4 potassium phosphate     -   KNO3 Potassium nitrate     -   LCMS Liquid Chromatography-Mass Spectrometry     -   Me3SiCl Trimethylsilyl chloride     -   MeOH Methanol     -   mg miligramme     -   MgSO4 Magnesium sulphate     -   min minute     -   mL mililiter     -   μL microliter     -   mmol milimol     -   MOG Myelin Oligodendrocyte Glycoprotein     -   mp melting point     -   N2 Nitrogen     -   NAFLD non-alcoholic fatty liver disease     -   NaHCO3 Sodium bicarbonate     -   NaOH Sodium hydroxide     -   NaOtBu Sodium tert-butoxide     -   NASH NonAlcoholic SteatoHepatitis     -   NH4Cl ammonium chloride     -   NMR nuclear magnetic resonance     -   NR Nuclear Receptor     -   PBC Primary Biliary Cholangitis     -   PCR Polymerase Chain Reaction     -   Pd/C Palladium on activated charcoal     -   Pd2(dba)3 Tris(dibenzylideneacetone)dipalladium(0)     -   Pd(OAc)2 Palladium(II) acetate     -   PMA Phorbol 12-Myristate 13-Acetate     -   ppm parts-per-million     -   PSC Primary Sclerosing Cholangitis     -   RA Rheumatoid Arthritis     -   ROR Retinoic Acid-Related Orphan Receptor     -   RPMI Roswell Park Memorial Institute medium     -   rt room temperature     -   sat. saturated     -   SIRS systemic inflammatory response syndrome     -   SPF Specific Pathogen Free     -   tBuOH tert-butanol     -   tBuXPhos 2-Di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl     -   Th17 T helper 17     -   THF TetraHydroFuran     -   TLC Thin-Layer Chromatography     -   UV ultra-violet     -   XantPhos 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene     -   XPhos Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl

FIGS. 1 and 2—Intermediate compounds for the synthesis of the Compounds of formula (I) or (Ia)

Intermediates are independently generated for the synthesis of compounds of formula (I) or (Ia): for example 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetic acid Ex. 1 (FIG. 1AA), 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid Ex. 3 (FIG. 1AB), 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetic acid Ex. 4 (FIG. 1AC), 2-[2-fluoro-5-(morpholin-4-yl)phenyl]acetic acid Ex. 7 (FIG. 1AD), 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid Ex. 10 (FIG. 1AE), 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetic acid Ex. 17 (FIG. 1AF), 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid Ex. 19 (FIG. 1AG), 2-[6-(morpholin-4-yl)pyridin-3-yl]acetic acid Ex. 22 (FIG. 1AH), 2-[2-(morpholin-4-yl)pyrimidin-5-yl]acetic acid Ex. 23 (FIG. 1AI), 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetic acid Ex. 24 (FIG. 1AJ), 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]acetic acid Ex. 26 (FIG. 1AK), 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]acetic acid Ex. 27 (FIG. 1AL), 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 28 (FIG. 1AM), 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 29 (FIG. 1AN), 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetic acid Ex. 30 (FIG. 1AO), 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetic acid Ex. 31 (FIG. 1AP), 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methylpropanoic acid Ex. 32 (FIG. 1AQ), 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclobutane-1-carboxylic acid Ex. 33 (FIG. 1AR), 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetic acid Ex. 36 (FIG. 1AS), 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Ex. 37 (FIG. 1AT) 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 41 (FIG. 1AU), 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]acetic acid Ex. 43 (FIG. 1AV), 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]acetic acid Ex. 44 (FIG. 1AW), 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]acetic acid Ex. 45 (FIG. 1AX), 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetic acid Ex. 46 (FIG. 1AY), 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1-carboxylic acid Ex. 49 (FIG. 1AZ), 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1-carboxylic acid Ex. 50 (FIG. 1BA), 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1-carboxylic acid Ex. 51 (FIG. 1BB), 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1-carboxylic acid Ex. 52 (FIG. 1BC) and 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxylic acid Ex. 53 (FIG. 1BD). In a same manner were synthetised:

-   -   [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methanamine         hydrochloride Ex. 11,         (2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 12,         (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine Ex. 20,         (5-chlorofuran-2-yl)(2,4-dimethylphenyl)methanamine Ex. 47 and         (5-chlorofuran-2-yl)(4-methylphenyl)methanamine hydrochloride         Ex. 48 (FIG.         2A)[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2-yl)methanamine         hydrochloride Ex. 13,         {4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 14,         2-[amino(5-methylfuran-2-yl)methyl]-5-methoxy-N,N-dimethylaniline         hydrochloride Ex. 15,         (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 16,         [5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methanamine         hydrochloride Ex. 18,         (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)         methanamine hydrochloride Ex. 21,         (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 25,         (4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 34, and         [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methanamine         Ex. 35,         (4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methanamine         hydrochloride Ex. 34,         (4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methanamine Ex. 38,         (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine Ex. 39,         (2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methanamine Ex. 40         (FIG. 2B)

FIG. 3—General synthesis scheme of Compounds of formula (I) or (Ia)

Compounds of formula (I) or (Ia) are generated using the Protocol A summarized in FIG. 3.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides novel compounds that are modulators of RORgamma. These compounds, and pharmaceutical compositions comprising the same, are suitable for treating any disease wherein the RORgamma activity is involved, for instance in multiple autoimmune, inflammatory, metabolic, fibrotic and cholestatic disorders.

The compounds according to the invention have the following formula (I):

in which,

R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, or a heterocyclic group;

R1b is a hydrogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkyl group or a heterocyclic group;

R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, a heterocyclic group, a cyano group, an amido group or a hydroxyl group;

R1d and R1e are, independently, a hydrogen atom, a halogen atom, a (C1-C6)alkyloxy group or a (C1-C6)alkyl group;

R2 is a (C1-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group or a heterocyclic group, optionally substituted by a (C1-C6)alkyl group;

R′2 is a hydrogen atom, a (C1-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group or a heterocyclic group, optionally substituted by a (C1-C6)alkyl group;

or R2 and R′2 can form, together with the carbon atom to which they are attached, a cycloalkyl group or a heterocycloalkyl group;

L1 is a NR7-CO—CH2, NR7-CO—, NR7-CO—C(CH3)2, CO—NH—CH2, CO—NH or CO—NH—C(CH3)2 group;

R7 represents a hydrogen atom or a (C1-C6)alkyl group;

L2 represents a bond, a (C1-C6)alkyl group, a (C3-C14)cycloalkyl group, or a CR8R′8 group;

R8 and R′8 are independently, a hydrogen atom, or a (C1-C6)alkylgroup;

R8 and R′8 can form, together with the carbon atom to which they are attached, a cycloalkyl group;

X1, X2, X3, X4, X5 are, independently, a CH group, a C—R4 group, a C—X6 group or a nitrogen atom;

X6 represents a CH group or a nitrogen atom;

X7 represents a sulfur atom, a SO2 group, an oxygen atom or CH group; and

R4 is a hydrogen atom, an alkyl group, a halogen atom.

The invention also relates to a compound of formula (Ia) wherein:

in which,

R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, or a heterocyclic group;

R1b is a hydrogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkyl group or a heterocyclic group;

R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, a heterocyclic group, a cyano group, an amido group or a hydroxyl group;

R1d and R1e are, independently, a hydrogen atom, a halogen atom, a (C1-C6)alkyloxy group or a (C1-C6)alkyl group;

wherein at least one R1a, R1b, R1c, R1d, and R1e is not a hydrogen atom;

R2 is a (C3-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group optionally substituted by a (C1-C6)alkyl group or by a halogen atom;

R′2 is a hydrogen atom, a (C1-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group, optionally substituted by a (C1-C6)alkyl group,

or R2 and R′2 can form, together with the carbon atom to which they are attached, a cycloalkyl group or a heterocycloalkyl group;

L1 is a NR7-CO—CH2, NR7-CO—, NR7-CO—C(CH3)2, CO—NH—CH2, CO—NH or CO—NH—C(CH3)2 group;

R7 represents a hydrogen atom or a (C1-C6)alkyl group;

L2 represents a bond, a (C1-C6)alkyl group, a (C3-C14)cycloalkyl group, or a CR8R′8 group;

with the proviso that when L1 is a NR7-CO— or a CO—NH group, L2 represents a (C1-C6)alkyl group, a (C3-C14)cycloalkylgroup, or a CR8R′8 group;

R8 and R′8 are independently, a hydrogen atom, or a (C1-C6)alkylgroup;

R8 and R′8 can form, together with the carbon atom to which they are attached, a cycloalkyl group;

X1, X2, X3, X4, X5 are, independently, a carbon or a nitrogen atom;

X6 represents a CH group or a nitrogen atom;

X7 represents a sulfur atom, a SO2 group, or an oxygen atom;

R4 is a hydrogen atom; an alkyl group optionally substituted by a hydroxy group or an alkoxy group; a halogen atom; an alkyloxy group or a hydroxy group.

The present invention also includes stereoisomers (diastereoisomers, enantiomers), pure or mixed, as well as racemic mixtures and geometric isomers, or tautomers of compounds of formula (I) or (Ia). The invention further includes salts, solvates (in particular hydrates) and polymorphs or crystalline forms of the compounds of formula (I) or (Ia).

According to a particular embodiment, the invention relates to a compound of formula (I) or (Ia) wherein R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group optionally substituted by at least one halogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, a piperidinyl group, a pyrrolidinyl group, a morpholinyl, an azabicyclohexanyl group, or an azepanyl group wherein said piperidinyl, pyrrolidinyl, azepanyl, or an azabicyclohexanylgroup can be optionally substituted by at least one (C1-C6)alkyl groups. In another particular embodiment, R1a is a hydrogen atom, a halogen, group, a (C1-C6)alkyl group optionally substituted by at least one halogen atom, a (C1-C6)dialkylamino group, a piperidinyl group (such as a piperidin-1-yl group), a morpholinyl group (such as morpholin-4-yl group), an azabicyclohexanyl group (such as a 3-azabicyclo[3.1.0]hexan-3-yl group) or an azepanyl group (such as a azepan-1-yl group).

In a particular embodiment, R1b is a hydrogen atom;

In a particular embodiment, R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, or a (C1-C6)alkyloxy group.

In another embodiment, R1d is a hydrogen atom or a (C1-C6)alkyl group. In another embodiment, R1d is a hydrogen atom.

In another embodiment, R1e is a hydrogen atom.

In another embodiment, R2 is a (C1-C6)alkyl group (such as a methyl, ethyl, propyl or butyl group, such as a isobutyl group), an aryl group or a heteroaryl group. In a further embodiment, R2 is a phenyl group or a substituted or unsubstituted furanyl group, such as a 5-methylfuran-2-yl or 5-chlorofuran-2-yl group.

In another embodiment, R′2 is a hydrogen atom.

In another particular embodiment, R2 is a (C1-C6)alkyl group (such as a methyl, ethyl, propyl or butyl group, such as a isobutyl group), an aryl group or a heteroaryl group, such as a phenyl group or a substituted or unsubstituted furanyl group, such as a 5-methylfuran-2-yl or 5-chlorofuran-2-yl group, and R′2 is a hydrogen atom.

In a particular embodiment, X6 is a nitrogen atom and X7 is a SO2 group or an oxygen atom. In a preferred embodiment, X6 is a nitrogen atom and X7 is a SO2 group.

In a particular embodiment, the cycle

is a substituent of X1, X2 or X3, in particular X3 (i.e. in para position of the L1-L2 group), and X2 (i.e. in meta position of the L1-L2 group).

In a particular embodiment, R4 a hydrogen atom, a (C1-C6)alkyl group, a (C1-C6)alkoxygroup, a hydroxyl group, or a halogen atom. In a further particular embodiment, R4 is a hydrogen atom; a methyl group optionally substituted by an alkoxy group or a hydroxy group; a methoxy group or a halogen atom.

In a particular embodiment, L1 is a NR7-CO—CH2, NR7-CO—C(CH3)2, CO—NH—CH2, or CO—NH—C(CH3)2 group.

In a particular embodiment, L2 is a bond.

In a particular embodiment, L1 is a NR7-CO—CH2, NR7-CO—C(CH3)2, CO—NH—CH2, or CO—NH—C(CH3)2 group and L2 is a bound. In a further particular embodiment, L1 is a NR7-CO—CH2 group. In another particular embodiment, R7 is a hydrogen atom.

In a particular embodiment, L1 is a NR7-CO— group and L2 is a CR8R′8 group. In a further particular embodiment, L1 is a NR7-CO— group wherein R7 is a hydrogen atom and L2 is a CR8R′8 group wherein R8 and R′8 form, together with the carbon atom to which they are attached, a cycloalkyl group, preferably a cyclopropyl of formula (III) or a cyclobutyl of formula (IV)

In a particular embodiment, L1 is a —NH—CO—CH2— group and L2 is a bond. In another embodiment, L1 is a or a —NH—CO— group and L2 is a CR8R′8 group wherein R8 and R′8 form, together with the carbon atom to which they are attached, a cycloalkyl group of formula (III).

In a further particular embodiment, the invention relates to a compound of formula (I) or (Ia) wherein:

R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, a piperidinyl group, a pyrrolidinyl group, a morpholinyl group, an azabicyclohexanyl group or an azepanyl group, wherein said piperidinyl, pyrrolidinyl, morpholinyl, azabicyclohexanyl or azepanyl group can be optionally substituted by at least one (C1-C6)alkyl groups;

R1b is a hydrogen atom;

R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, or a (C1-C6)alkyloxy group;

R2 is an aryl group, or a heteroaryl group, and R′2 is a hydrogen atom.

In a particular embodiment, the invention relates to a compound of formula (I) or (Ia), in which:

R1a is a halogen atom, (such as brome), a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group, such methyl group can be substituted by halogen atom such as a trifluoromethyl group), a (C1-C6)dialkylamino group (such as dimethylamino group or diethylamino group, in particular dimethylamino group), a piperidinyl group (such as a piperidin-1-yl group), a morpholinyl group (such as a morpholin-4-yl), an azabicyclohexanyl group (such as a 3-azabicyclo[3.1.0]hexan-3-yl group) or an azepanyl group (such as a azepan-1-yl group), wherein said piperidinyl, morpholinyl, azabicyclohexanyl or azepanyl group can be optionally substituted by at least one (C1-C6)alkyl groups;

R1b is a hydrogen atom;

R1c is a hydrogen, a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group), or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group);

R1d and R1e are hydrogen atoms;

R2 is a phenyl group or a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group);

L1 represents a NH—CO—CH2 group;

R4 is a hydrogen atom, a halogen atom (such as a fluor atom), a (C1-C6)alkyl group (such as a methyl group or an ethyl group, in particular a methyl group), a (C1-C6)alkyl group substituted by an alkoxy group or a hydroxyl group (such as a CH2OCH3 group or a CH2OH group) or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group);

the cycle

is a substituent of X1, X2 or X3, in particular X3 (in para position of the L1-L2 group) or X2 (in meta position of the L1-L2 group.

X6 is a nitrogen atom and X7 is a SO2 group or an oxygen atom.

In a particular variant of this embodiment, L2 is a bond.

In a particular embodiment, the invention relates to a compound of formula (I) or (Ia), in which:

R1a is a heterocyclic group (in particular a piperidinyl group (such as a piperidin-1-yl group));

R1c is a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group);

R2 is a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group);

L1 represents a NH—CO—CH2 group;

R4 is a hydrogen atom;

the cycle

is a substituent of X1, X2 or X3, in particular X3 (in para position of the L1-L2 group) or X2 (in meta position of the L1-L2 group; and

X6 is a nitrogen atom and X7 is a SO2 group.

In a particular variant of this embodiment, L2 is a bond.

In a particular embodiment, the invention relates to a compound of formula (I) or (Ia), in which:

R1a is a halogen atom (such as bromine atom), a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group, such methyl group being optionally substituted by at least one halogen atom such as a trifluoromethyl group), a (C1-C6)dialkylamino group (such as dimethylamino group or diethylamino group, in particular dimethylamino group), a piperidinyl group (such as a piperidin-1-yl group), a morpholinyl group (such as a morpholin-4-yl), an azabicyclohexanyl group (such as a 3-azabicyclo[3.1.0]hexan-3-yl group) or an azepanyl group (such as a azepan-1-yl group), wherein said piperidinyl, morpholinyl, azabicyclohexanyl or azepanyl group can be optionally substituted by at least one (C1-C6)alkyl groups;

R1b is a hydrogen atom;

R1c is a hydrogen, a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group), or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group);

R1d and R1e are hydrogen atoms;

R2 is a phenyl group, a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group), or a (C1-C6)alkyl group;

L1 represents a NR7-CO— group;

R7 is a hydrogen atom;

L2 represents a CR8R′8 group (such as a cyclopropyl group of formula (III) or cyclobutyl of formula (IV)

in particular L2 is a cyclopropyl group of formula (III);

R4 is a hydrogen atom, a halogen atom (such as a bromine atom), a (C1-C6)alkyl group (such as a methyl group or an ethyl group, in particular a methyl group), or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group);

the cycle

is a substituent of X1, X2 or X3, in particular X3 (in para position of the L1-L2 group) or X2 (in meta position of the L1-L2 group;

X6 is a nitrogen atom and X7 is a SO2 group.

In a particular embodiment, the invention relates to a compound of formula (I) or (Ia), in which:

R1a is a (C1-C6)alkyl group or a heterocyclic group (in particular a piperidinyl group (such as a piperidin-1-yl group));

R1c is a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group);

R2 is a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group);

L1 represents a NR7-CO— group;

R7 is a hydrogen atom;

L2 represents a CR8R′8 group (such as a cyclopropyl group of formula (III) or cyclobutyl of formula (IV)

in particular wherein L2 is a cyclopropyl group of formula (III);

R4 is a hydrogen atom;

the cycle

is a substituent of X1, X2 or X3, in particular X3 (in para position of the L1-L2 group) or X2 (in meta position of the L1-L2 group;

X6 is a nitrogen atom; and

X7 is a SO2 group.

In a particular embodiment:

R1a is a hydrogen atom, a halogen atom (such as bromine atome), a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group), a piperidinyl group (such as a piperidin-1-yl group) or an azabicyclohexanyl group (such as a 3-azabicyclo[3.1.0]hexan-3-yl group);

R1b is a hydrogen atom;

R1c is a halogen atom (such as a chlorine atom), a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group), or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group);

R1d and R1e are hydrogen atoms;

R2 is a phenyl group or a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group);

L1 represents a NH—CO— group;

L2 represents a CH2 group or a group of formula (III)

R4 represents a a hydrogen atom or a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group);

X6 is a nitrogen atom; and

X7 is a SO2 group.

In a particular embodiment:

R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, or a heterocyclic group;

R1b is a hydrogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkyl group or a heterocyclic group;

R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, a heterocyclic group, a cyano group, an amido group or a hydroxyl group;

R1d and R1e are, independently, a hydrogen atom, a halogen atom, a (C1-C6)alkyloxy group or a (C1-C6)alkyl group;

wherein at least one R1a, R1b, R1c, R1d, and R1e is not a hydrogen atom;

R2 is a (C3-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group optionally substituted by a (C1-C6)alkyl group or by a halogen,

R′2 is a hydrogen atom, a (C1-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group, optionally substituted by a (C1-C6)alkyl group,

or R2 and R′2 can form, together with the carbon atom to which they are attached, a cycloalkyl group or a heterocycloalkyl group;

L1 is a NR7-CO—, or CO—NH— group;

R7 represents a hydrogen atom or a (C1-C6)alkyl group;

L2 represents a (C4-C6)alkyl group, a (C3-C14)cycloalkyl group, or a CR8R′8 group;

R8 and R′8 are independently, a hydrogen atom, or a (C1-C6)alkylgroup;

R8 and R′8 can form, together with the carbon atom to which they are attached, a cycloalkyl group;

X1, X2, X3, X4, X5 are, independently, a carbon or a nitrogen atom;

X6 represents a CH group or a nitrogen atom;

X7 represents a sulfur atom, a SO2 group, an oxygen atom.

R4 is a hydrogen atom; an alkyl group optionally substituted by a hydroxy group or an alkoxy group; a halogen atom; an alkyloxy group or a hydroxy group.

In particular embodiments, in the compound of formula (I) or (Ia) of the present invention:

a (C1-C6)alkyl group may be a substituted or unsubstituted (C1-C6)alkyl group, in particular a substituted or unsubstituted (C1-C4)alkyl group;

a (C1-C6)alkyloxy group may be a substituted or unsubstituted (C1-C6)alkyloxy group, in particular a substituted or unsubstituted (C1-C4)alkyloxy group;

a (C6-C14)aryl group may be a substituted or unsubstituted (C6-C14)aryl group;

a heterocyclic group may be a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

The term “alkyl” refers to a saturated hydrocarbon radical that is linear or branched, substituted or not, having preferably from one to six, and even more preferably from one to four carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, or sec-butyl. The alkyl group can be optionally substituted by one or more halogen atoms, by a (C6-C14)aryl group or by a (C3-C14)cycloalkyl group. Further possible substituents of an alkyl group also include one or more substituents selected from a —NH2 group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, a hydroxy, an alkyloxy and a (C2-C6)alkynyl group.

The term alkynyl denotes linear or branched hydrocarbon groups containing from 2 to 6 carbon atoms and containing at least one triple bond. Examples of alkynyl containing from 3 to 6 carbon atoms are 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl and the isomeric forms thereof.

The terms “alkyloxy” and “alkylthio” refer to an alkyl group as defined above that is linked to the remainder of the compound by an oxygen or sulfur atom, respectively.

The term “(C1-C6)alkylamino” refers to a —NH—(C1-C6)alkyl group. In a particular embodiment, the alkyl group of the alkylamino group may be substituted or not with a (C3-C14)cycloalkyl group, a (C6-C14)aryl group, a heterocyclic group, or a (C1-C6)alkyloxycarbonyl group.

The term “(C1-C6)dialkylamino” refers to a —NRR′ group where R and R′ independently represent a (C1-C6)alkyl group as defined above. In a particular embodiment, the alkyl groups of the dialkylamino group may independently be substituted or not with a (C3-C14)cycloalkyl group, a (C6-C14)aryl group, a heterocyclic group, or a (C1-C6)alkyloxycarbonyl group.

The term “cycloalkyl” designates a substituted or unsubstituted alkyl group that forms one cycle having preferably from three to fourteen carbon atoms, and more preferably five to six carbon atoms, such as cyclopropyl, cyclopentyl and cyclohexyl. The cycloalkyl group of the present invention may be unsubstituted, or substituted, for example with a (C1-C6)alkyl group, in particular with a (C1-C6)alkyl group substituted with one or more halogen atoms, such as the CF3 group.

The term “cycloalkylamino” refers to a —NH—(C3-C14)cycloalkyl group or a —N((C1-C6)alkyl)(C3-C14)cycloalkyl group.

The term “amino group” designates a —NH2 group.

The term “hydroxyl group” refers to a —OH group.

The term “carbonyl” designates a CO group.

The term “carbonyl(C1-C6)alkyl” designates a CO—(C1-C6)alkyl group.

The term “amido” designates a CO—NH2 group.

The term “alkylamido” designates a CO—NH—(C1-C6)alkyl group.

The term “(C1-C6)dialkylamido” designates a CO—NRR′ group, R and R′ representing a (C1-C6)alkyl group as defined above.

A sulfone group designates a SO2 group;

The term “aryl” designates an aromatic group, substituted or not, having preferably from six to fourteen carbon atoms such as phenyl, a-naphtyl, b-naphtyl, or biphenyl.

The term “heterocyclic” refers to a heterocycloalkyl group or a heteroaryl group. The term “heterocycloalkyl” group refers to a cycloalkyl as indicated above that further comprises one or several heteroatoms selected among nitrogen, oxygen or sulfur. They generally comprise from four to fourteen carbon atoms, such as morpholinyl, piperazinyl, piperidinyl, pyrrolidinyl, tetrahydropyranyl, dithiolanyl and azepanyl groups. In a particular embodiment, the heterocycloalkyl group is a 5-, 6- or 7-membered cycle. The term “heteroaryl” refers to an aryl group as indicated above, substituted or not, that further comprises one or several heteroatoms selected among nitrogen, oxygen or sulfur. They generally comprise from four to fourteen carbon atoms. In a particular embodiment, the heteroaryl group is a 5-, 6- or 10-membered heteroaryl group. Representative heteroaryl groups include a pyridinyl, pyrimidinyl, furanyl, thiophenyl, quinoleinyl, and isoquinoleinyl group.

The aryl group or the heterocyclic group can be optionally substituted by one or more halogen atom(s), (C1-C6)alkyl group(s), or (C1-C6)alkyloxy group(s). By halogen atom, an atom of bromine, chlorine, fluorine or iodine is understood, in particular an atom of bromine, chlorine or fluorine.

Specific compounds according to the invention include:

-   Cpd. 1:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; -   Cpd. 2:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; -   Cpd. 3:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; -   Cpd. 4:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]-N-{[4-methyl-2-(morpholin-4-yl)phenyl](phenyl)methyl}acetamide; -   Cpd. 5:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 6:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 7:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(morpholin-4-yl)phenyl](phenyl)methyl}acetamide; -   Cpd. 8:     2-[2-fluoro-5-(morpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](phenyl)methyl}acetamide; -   Cpd. 9:     N-[(2-bromo-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetamide; -   Cpd. 10:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 11:     N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; -   Cpd. 12:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 13:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 14:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-({4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methyl)acetamide; -   Cpd. 15:     N-{[2-(dimethylamino)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; -   Cpd. 16:     N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; -   Cpd. 17:     2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide;

Cpd. 18: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide;

-   Cpd. 19:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; -   Cpd. 20:     2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 21:     N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; -   Cpd. 22:     N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetamide; -   Cpd. 23:     N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; -   Cpd. 24:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 25:     N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}-2-[6-(morpholin-4-yl)pyridin-3-yl]acetamide; -   Cpd. 26:     N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}-2-[2-(morpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 27:     2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 28:     N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; -   Cpd. 29:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 30:     2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 31:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 32:     1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; -   Cpd. 33:     2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 34:     N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 35:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 36:     N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 37:     1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; -   Cpd. 38:     2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 39:     2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 40:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methylpropanamide; -   Cpd. 41:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclobutane-1-carboxamide; -   Cpd. 42:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetamide; -   Cpd. 43:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetamide; -   Cpd. 44:     1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methyl]cyclopropane-1-carboxamide; -   Cpd. 45:     N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 46:     N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 47:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 48:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; -   Cpd. 49:     N-[(R4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 50:     N-[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 51:     N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; -   Cpd. 52:     N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; -   Cpd. 53:     N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; -   Cpd. 54:     N-[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; -   Cpd. 55:     1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclobutane-1-carboxamide; -   Cpd. 56:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methyl-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}propanamide; -   Cpd. 57:     1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methyl]cyclopropane-1-carboxamide; -   Cpd. 58:     1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; -   Cpd. 59:     1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[3-methyl-1-[2-(piperidin-1-yl)phenyl]butyl]cyclopropane-1-carboxamide; -   Cpd. 60:     1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[(5-methylfuran-2-yl)[2-(piperidin-1-yl)phenyl]methyl]cyclopropane-1-carboxamide; -   Cpd. 61:     2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 62:     2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 63:     2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 64:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 65:     2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; -   Cpd. 66:     N-[(5-chlorofuran-2-yl)(2,4-dimethylphenyl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 67:     N-[(5-chlorofuran-2-yl)(4-methylphenyl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 68:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; -   Cpd. 69:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1-carboxamide; -   Cpd. 70:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1-carboxamide; -   Cpd. 71:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1-carboxamide; -   Cpd. 72:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1-carboxamide;     and -   Cpd. 73:     N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxamide.

In the present invention, the terms “RORgamma”, “RORγ” and “RORg” are used interchangeably.

“RORγ modulator” refers to a chemical compound that modulates, either directly or indirectly, the activity of RORγ. In particular, the RORγ modulator modulates, in particular inhibits or activates, more particularly inhibits, either directly or indirectly, the activity of RORγ. RORγ modulators include antagonists, inverse agonists and agonists of RORγ, in particular antagonists and inverse agonists.

RORgamma modulators can be used as medicinal products. Consequently, the present invention provides a compound of formula (I) or (Ia) for use as a medicament.

The present invention further provides a pharmaceutical composition comprising a compound of formula (I) or (Ia) and a pharmaceutically acceptable carrier. A compound of formula (I) or (Ia), optionally in combination with one or more other therapeutically active substances, may be used in methods for treating diseases for which the modulation of RORgamma has positive effects in a subject in need thereof.

The present invention further provides a compound of formula (I) or (Ia) for use in the treatment of a RORγ related-disease. The invention also provides a method for treating a RORγ related-disease comprising the administration of a therapeutically effective amount of a compound of formula (I) or (Ia) to a subject in need thereof. The invention further provides the use of a compound of formula (I) or (Ia), in the manufacture of a medicament for use in the treatment of a RORγ related-disease.

The compounds of the invention may in particular be used in the treatment of a RORγ related-disease such as an autoimmune or autoimmune-related disease, inflammation-related disease, metabolic disease and/or fibrotic disease, cholestatic, cholestasis-related disease or a cancer. In a particular embodiment, the compound of formula (I) or (Ia) is used in the treatment of an autoimmune or autoimmune-related disease, an inflammation-related disease, a metabolic disease, a fibrotic disease, a cholestatic disease or a cholestasis-related disease.

The term “autoimmune disease” is used to designate a condition that arises from an abnormal immune response of the body against substances and tissues normally present in the body. The disease may be restricted to certain organs (e.g pancreas, in type I diabetes or thyroid gland in autoimmune thyroiditis) or involve a particular tissue in different places (e.g. in Goodpasture's disease, affection of the basement membrane in the lung and the kidney).

The term “inflammation” is used to designate a condition that arise from a protective response involving host cells, blood vessels, and proteins and other mediators which may serve to eliminate the cause of cell/tissue injury, as well as the necrotic cells/tissues resulting from the original insult, and to initiate the process of repair. The inflammatory reaction may be manifested by pain, heat, redness, swelling, blood vessels dilatation, blood flow increase and loss of function.

Fibrosis is a pathologic process, which includes scar formation and over production of extracellular matrix, by the connective tissue, as a response to tissue damage. Damage to tissue can result from a variety of stimuli including autoimmune reactions and mechanical injury. This can be a reactive, benign, or pathological state that occurs in an organ or tissue. In response to injury this is called scarring and if fibrosis arises from a single cell line this is called a fibroma. Physiologically the deposit of connective tissue can obliterate the architecture and function of the underlying organ or tissue.

Cholestasis is defined as a decrease in bile flow due to impaired secretion by hepatocytes (hepato-cellular cholestasis) or to obstruction of bile flow through intra- or extrahepatic bile ducts (obstructive cholestasis). In clinical practice, cholestasis is any condition in which the flow of bile from the liver is slowed or blocked.

Cancers are a large family of diseases that involve abnormal cell growth with the potential to invade or spread to other parts of the body. IL-17, which is produced by several types of cells, including immune cells, where IL-17 expression relies on RORgt, is known to contribute to malignant transformation and metastasis of several cancers.

Examples of autoimmune diseases, autoimmune-related diseases, inflammatory diseases, metabolic diseases, fibrotic diseases, cholestatic diseases and cancers include arthritis, asthma, severe, glucocorticoid-nonresponsive asthma, asthma exacerbations due to ongoing and/or past pulmonary infection, Addison's disease, allergy, agammaglobulinemia, alopecia areata, ankylosing spondylitis, atherosclerosis, atopic allergy, atopic dermatitis, autoimmune cardiomyopathy, autoimmune enteropathy, autoimmune hemolytic anemia, autoimmune hepatitis, autoimmune lymphoproliferative syndrome, autoimmune pancreatitis, autoimmune peripheral neuropathy, Crohn's disease, Celiac disease, colitis, chronic inflammatory demyelinating polyneuropathy, chronic obstructive pulmonary disease (COPD), dermatomyositis, diabetes mellitus type 1, diffuse cutaneous systemic sclerosis, eczema, gastrointestinal disorder, Goodpasture's syndrome, Graves' disease, Guillain-Barre syndrome, Hashimoto's encephalopathy, Hashimoto's thyroiditis, idiopathic thrombocytopenic purpura, inflammatory bowel disease (IBD), irritable bowel syndrome, lupus, lupus erythematosus, lupus nephritis, mixed connective tissue disease, Kawasaki disease, multiple sclerosis, neuromyelitis optica, myasthenia gravis, narcolepsy, optic neuritis, osteorathritis, pemphigus vulgaris, pernicious anaemia, polymyositis, psoriasis, psoriatic arthritis, reactive arthritis, relapsing polychondritis, respiratory disorder, rheumatoid arthritis, rheumatic fever, Sjorgen's syndrome, systemic lupus erythematosus, transverse myelitis, undifferentiated connective tissue disease, ulcerative colitis, uveitis, vasculitis, Wegener's granulomatosis, systemic inflammatory response syndrome (SIRS), sepsis, Behcets disease, allergic contact dermatitis, cutaneous lupus erythematosus, dry eye and glomerulonephritis, myocarditis, acute liver failure (ALF), including acute-on-chronic liver failure (ACLF), pulmonary fibrosis (idiopathic pulmonary, interstitial lung, cystic and progressive massive fibrosis), liver fibrosis and cirrhosis of diverse etiologies (congenital, of autoimmune origin, induced by cardiometabolic diseases, alcohol consumption, cholestasis, drugs, infectious agents, trauma, radiation), metabolic syndrome, non-alcoholic fatty liver disease (NAFLD), NonAlcoholic SteatoHepatitis (NASH) and Alcoholic SteatoHepatitis (ASH), cardiac fibrosis and heart myocardial and endomyocardial fibrosis, arterial fibrosis, atherosclerosis/restenosis, mediastinal fibrosis (soft tissue of the mediastinum), macular degeneration, retinal and vitreal retinopathy, ocular scarring, cataract, Alzheimer's disease, cancer, local, disseminated or metastatic cancer, scleroderma, glioblastoma, myelofibrosis (bone marrow), retroperitoneal fibrosis (soft tissue of the retroperitoneum), nephrogenic systemic fibrosis (skin, joints, eyes, and internal organs), keloid (skin), intestinal fibrosis (occurs for example in Crohn's disease and collagenous colitis), kidney fibrosis, scleroderma and systemic sclerosis (skin, lungs, kidneys, heart, and gastrointestinal tract), arthrofibrosis (knee, shoulder, other joints), Peyronie's disease (penis), Dupuytren's contracture (hands and fingers), some forms of adhesive capsulitis (shoulder), obesity, Primary Biliary Cholangitis (PBC), Primary Sclerosing Cholangitis (PSC), Intarhepatic Cholestasis of Pregnancy (ICP), Progressive Familial Intrahepatic Cholestasis (PFIC), Biliary atresia, Cholelithiasis, Infectious cholangitis, Cholangitis associated with Langerhans cell histiocytosis, Alagille syndrome, Nonsyndromic ductal paucity, Hepatitis (hepatitis A, hepatitis B, hepatitis C), Alphal-antitrypsin deficiency, Inborn errors of bile acid synthesis, Drug-induced cholestasis, Total parenteral nutrition (TPN)-associated cholestasis, breast cancer and breast cancer metastasis, pancreatic cancer and pancreatic cancer metastasis, pancreatic ductal adenocarcinoma, liver cancer and liver cancer metastasis, hepatocellular carcinoma, lung cancer and lung cancer metastasis, non-small-cell lung cancer, colorectal cancer and colorectal cancer metastasis, colorectal carcinoma, prostate cancer and prostate cancer metastasis, gallbladder cancer and gallbladder cancer metastasis.

In particular, RORg modulators may be used in the treatment of asthma, ankylosing spondylitis, autoimmune cardiomyopathy, autoimmune hepatitis, crohn's disease, chronic obstructive proliferative disease (COPD), diabetes mellitus type 1, lupus erythematosus, lupus nephritis, multiple sclerosis, psoriasis, psoriatic arthritis, rheumatoid arthritis, ulcerative colitis, myocarditis, pulmonary fibrosis (idiopathic pulmonary, interstitial lung, cystic and progressive massive fibrosis), non-alcoholic fatty liver disease (NAFLD), non-alcoholic steato-hepatitis (NASH) and alcoholic steatoHepatitis (ASH), cardiac fibrosis and heart myocardial and endomyocardial fibrosis, arterial fibrosis, atherosclerosis/restenosis, intestinal fibrosis (occurs for example in crohn's disease and collagenous colitis), kidney fibrosis, scleroderma, systemic sclerosis, primary biliary cholangitis (PBC), hepatitis (hepatitis A, hepatitis B, hepatitis C), colon cancer, small-cell lung cancer, non-small cell lung cancer, prostate cancer, renal cancer, ovarian cancer, bladder cancer, stomach cancer, liver cancer, testis cancer, uterus cancer, leukemia, adenocarcinoma, melanoma and cancer of central nervous system tissue.

The term “treatment” or “treating” refers to therapy, prevention, or prophylaxis of a disorder in a subject in need thereof. The treatment involves the administration of a pharmaceutical composition to subjects (e.g. patients) having a declared disorder to prevent, cure, delay, reverse, or slow down the progression of the disorder, improving thereby the condition of patients. A treatment may also be administered to subjects that are either healthy or at risk of developing a disorder such as an autoimmune, inflammatory, fibrotic or cholestatic disorder.

The term “subject” refers to a mammal and more particularly a human. The subjects to be treated according to the invention can be appropriately selected on the basis of several criteria associated with autoimmune, inflammatory, fibrotic and cholestatic pathological processes such as previous and/or present drug treatments, associated pathologies, genotype, exposure to risk factors, as well as any other relevant biomarker that can be evaluated by means of any suitable immunological, biochemical, or enzymatic method.

The Examples show how Compounds of formula (I) or (Ia) can be produced and tested.

The details of the general methods of synthesis and purification of intermediate products for Compounds of formula (I) or (Ia) are provided in Example 1.

Specific reaction intermediates can be synthesized and purified from compounds that may be already available commercially or that can be readily synthesized.

The details of the general methods of synthesis and purification of Compounds of formula (I) or (Ia) are provided in Example 2.

General schemes of synthesis of the compounds of formula (I) or (Ia) are presented in FIG. 3A.

The functional groups optionally present in the reaction intermediates that are generated for obtaining the desired compounds of formula (I) or (Ia) can be protected, either permanently, or temporarily, by protective groups, which ensure unequivocal synthesis of the desired compounds. The reactions of protection and deprotection are carried out according to techniques well known by a person skilled in the art or such as those described in the literature, as in the book “Greene's Protective Groups in Organic Synthesis” (Wuts & Greene, 2007).

The compounds according to the invention may contain one or more asymmetric centers. The present invention includes stereoisomers (diastereoisomers, enantiomers), pure or mixed, as well as racemic mixtures and geometric isomers, or tautomers of compounds of formula (I) or (Ia). When an enantiomerically pure (or enriched) mixture is desired, it can be obtained either by purification of the final product or of chiral intermediates, or by asymmetric synthesis according to methods known by a person skilled in the art (using for example chiral reactants and catalysts). Certain compounds according to the invention can have various stable tautomeric forms and all these forms and mixtures thereof are included in the invention. The techniques for obtaining and characterizing the stereoisomers, pure or mixed, as well as racemic mixtures and geometric isomers, or tautomers are described in the literature, such as in the book “Chirality in Drug Design and Development” (Reddy & Mehvar, 2004).

The compounds of formula (I) or (Ia) can be purified by precipitation or solid/liquid extraction after evaporation of the reaction medium. Further or other purification step can be performed by chromatography over silica gel or by crystallization, when the compound is stable as a solid form, by applying techniques well known in the literature or, more in general, for chemicals (Armarego & Chai, 2009).

Moreover, the required purification and/or (re-)crystallization steps that are appropriate for isolating compounds of formula (I) or (Ia) from the reaction mixture, can be used for obtaining amorphous, polymorphous, mono- or poly-crystalline forms. Such polymorphisms may present distinct pharmacological and/or chemical properties, for example in terms of solubility, intrinsic dissolution rate, melting temperature, bioavailability, and/or possible transition from a polymorphic state to another one in pharmaceutical compositions and/or biological fluids.

The (re-)crystallisation assays can be performed in panels of different solvents (such as isopropanol, acetone, methanol, diisopropyl ether or water) or mixture thereof, and by applying different conditions, such as reaction volumes or temperatures. The resulting samples can be analyzed by different techniques such as microscopy, calorimetry, and/or spectroscopy that allow establishing the features of a particular crystalline form, such as structure, solubility, stability or conversion to other forms (Bauer, 2004; Erdemir et al, 2007; Morissette et al, 2004; Yin & Grosso, 2008).

Such a polymorphism study allows characterizing the crystalline form of a compound that is pharmaceutically acceptable for both pharmacological and manufacturing points of view.

Certain compounds of formula (I) or (Ia) can be isolated in the form of zwitterions and each of these forms is included in the invention, as well as mixtures thereof.

Compounds of formula (I) or (Ia) and their salts can be stable in liquid or solid forms. The present invention includes all solid and liquid forms of formula (I) or (Ia), which includes the amorphous, polymorphic, mono- and poly-crystalline forms. In particular, the compounds of formula (I) or (Ia) can exist in the free form or in the solvated form, i.e. in the form of associations or combinations with one or more molecules of a solvent, for example with pharmaceutically acceptable solvents such as water (hydrates) or ethanol. The present invention also includes the prodrugs of the compounds according to the invention which, after administration to a subject, are converted to the compounds as described in the invention or to their metabolites having therapeutic activities comparable to the compounds according to the invention.

Specific compounds of formula (I) or (Ia) can comprise at least one atom of the structure that is replaced by an isotope (radioactive or not). Examples of isotopes that can be included in the structure of the compounds according to the invention can be selected from hydrogen, carbon, nitrogen, oxygen, sulphur such as ²H, ³H, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³⁵S respectively. When non-radioactive, the stable isotope can be selectively incorporated in the structure in place of hydrogen (in the case of deuterium) or carbon (in the case of ¹³C) not only as means of performing absorption, distribution, metabolism, and excretion (ADME) studies but also as means for obtaining compounds that may retain the desired biochemical potency and selectivity of the original compound while the metabolic fate is substantially altered. In some favourable cases, this modification has the potential to have a positive impact effect on safety, efficacy and/or tolerability of the original compound (Mutlib, 2008). Otherwise radioactive isotopes ³H and ¹⁴C are particularly preferred as they are easy to prepare and detect in studies of the bioavailability in vivo of the substances. The heavy isotopes (such as ²H) are particularly preferred as they are used as internal standards in analytical studies and as possible variants of pharmaceutical interest.

Compounds of formula (I) or (Ia) can be obtained as specific salts, hydrates, and polymorphs that can be obtained during the final purification step of the compound or, in the case of salts, by incorporating the salt into the previously purified compound. The selection of a compound of formula (I) or (Ia) that is produced according to the methods of the Invention as an optimal candidate for drug development can be automated for a comprehensive biopharmaceutical characterization at the scale-up stage and for the solid or liquid formulation that is appropriate for the desired route of administration and therapeutic indication (Kumar et al, 2007; Mahato & Narang, 2011; Stahl & Wermuth, 2002).

In view of their use as medicinal products, the compounds of formula (I) or (Ia) can be formulated as pharmaceutically acceptable salts obtained from organic or inorganic bases or acids of such compounds. Alternatively, the compounds of formula (I) or (Ia) can be formulated as pharmaceutically acceptable hydrates or polymorphs of such compounds. These salts, hydrates, and polymorphs can be obtained during the final purification step of the compound or, in the case of salts, by incorporating the salt into the previously purified compound (Stahl & Wermuth, 2002).

These salts can be prepared with pharmaceutically acceptable acids but the salts of other acids useful for purifying or isolating the compounds of formula (I) or (Ia) also form part of the invention. In particular, when the compounds according to the invention are in the form of a salt, it is a salt of an alkali metal, in particular a salt of sodium or of potassium, or a salt of an alkaline-earth metal, in particular magnesium or calcium, or a salt with an organic amine, more particularly with an amino acid such as arginine or lysine.

The present invention further provides pharmaceutical compositions comprising a compound of formula (I) or (Ia), or a pharmaceutically acceptable salt thereof, and optionally at least one pharmaceutically acceptable carrier or diluent. The pharmaceutical compositions comprising a compound of formula (I) or (Ia) may comprise one or several excipients or vehicles acceptable within a pharmaceutical context (e.g., for liquid formulations, saline solutions, physiological solutions, isotonic solutions).

A further object of the invention are methods of preparing such pharmaceutical compositions, comprising admixing a compound of formula (I) or (Ia), with at least one pharmaceutically acceptable carrier, vehicle, or diluent. These methods involve, for example, conventional mixing, dissolving, granulation, dragee-making, levigating, emulsifying, encapsulating, entrapping, lyophilizing processes or spray drying (Gennaro, 2000; Rowe et al, 2003).

The phrase “pharmaceutically acceptable” refers to those properties and/or substances that are acceptable to the patient from a pharmacological/toxicological point of view and to the manufacturing pharmaceutical chemist from a physical/chemical point of view regarding composition, formulation, stability, patient acceptance and bioavailability.

The term “carrier”, “vehicle”, or “excipient” refers to any substance, not itself a therapeutic agent, that is added to a pharmaceutical composition to be used as a carrier, vehicle, and/or diluent for the delivery of a therapeutic agent to a subject in order to improve its handling or storage properties or to permit or facilitate formation of a dosage unit of the composition into a discrete article. The pharmaceutical compositions of the invention, either individually or in combination, can comprise one or several agents or vehicles chosen among dispersants, solubilisers, stabilisers, preservatives, etc. Agents or vehicles useful for these formulations (liquid and/or injectable and/or solid) are particularly methylcellulose, hydroxymethylcellulose, polysorbate 80, mannitol, gelatin, lactose, vegetable oils, liposomes, etc. Acceptable excipients can be chosen among disintegrants, binding agents, adhesives, wetting agents, lubricants, glidants, flavors, dyes, fragrances, stearic acid, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, magnesium carbonate, talc, gelatin, lactose, sucrose, starches, polymers, such as polyvinyl alcohol and polyethylene glycols, and other pharmaceutically acceptable materials added to improve taste, odor or appearance of the composition.

The compounds can be made up in solid or liquid form, such as tablets, capsules, powders, syrups, elixirs and the like, aerosols, sterile solutions, suspensions or emulsions, and the like. The composition may be presented in a solid preformulation composition wherein the active ingredients are dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective dosage forms such as tablets, pills and capsules. Additionally, the combined compositions may be delivered using sustained-release formulations.

The compositions can be formulated as injectable suspensions, gels, oils, pills, suppositories, powders, gel caps, capsules, aerosols, etc., eventually by means of galenic forms or devices assuring a prolonged and/or slow release. For this kind of formulation, agents such as cellulose, carbonates or starches can advantageously be used. The compositions of the present invention can also be formulated in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes can be formed from a variety of lipids, including but not limited to amphipathic lipids such as phosphatidylcholines, sphingomyelins, phophatidylcholines, cardiolipins, phosphatidylethanolamines, phosphatidylserines, phosphatidylglycerols, phosphatidic acids, phosphatidylinositols, diacyl trimethylammonium propanes, diacyl dimethylammonium propanes, and stearylamine, neutral lipids such as triglycerides, and combinations thereof.

The pharmaceutical combination of the invention can be administered in a systematic or parenteral way, by using oral, topical, perlingual, nasal, rectal, transmucosal, transdermal, intestinal, intramuscular, intravenously, subcutaneous, intraarterial, intraperitoneal, intrapulmonary or intraocular route, by using methods known in the art.

Formulations for oral administration may be in the form of aqueous solutions and suspensions, in addition to solid tablets and capsule formulations. The aqueous solutions and suspensions may be prepared from sterile powders or granules. The compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, and/or various buffers.

For administration by inhalation, the pharmaceutical compositions comprising a compound of formula (I) or (Ia) are conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebulizer, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, 1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3,3-heptafluoropropane, carbon dioxide or other suitable gas, alone or in combination. Pressurized aerosols may be formulated as suspensions or solutions, and include an appropriate propellant formulation, and various excipients, such as surfactants, co-solvents, etc. In the case of a pressurized aerosol the dosage unit may be determined by providing a valve to deliver a metered amount. Capsules and cartridges of e.g. gelatin for use in an inhaler or insufflators may be formulated containing a powder mix of the compound and a suitable powder base such as lactose or starch.

The tablets or pills of the composition can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action. For example, the tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer that serves to resist disintegration in the stomach and permits the inner component to pass intact into the duodenum or to be delayed in release. A variety of material can be used for such enteric layers or coatings, such materials including a number of polymeric acids with such as shellac and cellulose acetate.

The liquid forms in which the pharmaceutical compositions can be incorporated for oral administration or by injection include, aqueous solutions, suitably flavoured syrups, aqueous or oil suspensions, and flavoured emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil or peanut oil, as well as elixirs and similar pharmaceutical vehicles. Suitable dispersing or suspending agents for aqueous suspensions, include synthetic and natural gums such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinyl-pyrrolidone or gelatin. The liquid forms in suitably flavored suspending or dispersing agents may also include the synthetic and natural gums, for example, tragacanth, acacia, methyl-cellulose and the like. For parenteral administration, sterile suspensions and solutions are desired. A person skilled in the art will take care to select the possible compound or compounds to be added to these compositions in such a way that the advantageous properties intrinsically attaching to the present invention are not or substantially not altered by the addition envisaged, as is also explained in the literature, for example in the book “Pharmaceutical Dosage Forms and Drug Delivery” (2007; edited by Mahato R; published by CRC Press).

A pharmaceutical composition as disclosed herein is understood to be useful for treating a RORγ related-disease, that is, the active ingredients are contained in an amount to achieve their intended purpose. At this scope, a compound of formula (I) or (Ia) should be administered in an effective amount by using a pharmaceutical composition as above-defined. Administration can be performed daily or even several times per day, if necessary, and in an amount that can be optimal or suboptimal, if they are compared with dosages that are normally used for such compounds.

The term “effective amount” refers to an amount of the compound sufficient to produce the desired therapeutic result. In particular the compounds of formula (I) or (Ia) are administered in amounts that are sufficient to display a desired effect.

Optimal dosages of compounds of formula (I) or (Ia) to be administered may be readily determined by those skilled in the art, and will vary with the particular compound used, the strength of the preparation, the mode of administration, and the severity of the condition to be treated. In addition, factors associated with the particular patient being treated, including patient age, weight, diet and time of administration, will result in the need to adjust dosages and interval. The frequency and/or dose relative to the simultaneous or separate administrations can be adapted by one of ordinary skill in the art, in function of the patient, the pathology, the form of administration, etc. For instance, a compound of formula (I) or (Ia) should be provided in a dosage that allows its administration in the amount 0.01 mg/day to 1000 mg/day, preferably from 0.1 mg/day to 10 mg/day.

The compounds of formula (I) or (Ia) can advantageously be formulated and/or administered in combination with one or more other therapeutically active substances, marketed or under development, that are selected according to a specific autoimmune, inflammatory, fibrotic or cholestatic disorder or any other disorders that may be found associated to said disorder in medical settings and that should be also treated. Such a combined administration includes two possibilities: the two agents are administered to a subject at substantially similar times; or the two agents are administered to a subject at different times, at independent intervals that may or may not overlap or coincide. As such, the invention also relates to a kit-of-parts, comprising a compound of the invention, in association with another therapeutically active agent, for their simultaneous, separate or sequential use in the therapy, in particular in the treatment of an autoimmune, inflammatory, fibrotic or cholestatic disorder.

The invention also relates to a pharmaceutical composition comprising a compound of formula (I) or (Ia) and at least one other therapeutically active agent.

A non-exhaustive list of active agents that may be advantageously formulated and/or administered with compounds of formula (I) or (Ia) includes:

-   -   anti-inflammatory;     -   anti-oxidant agents;     -   immunosuppressor agents;     -   agents used in the treatment of asthma;     -   agents used in the treatment of psoriasis;     -   agents used in the treatment of respiratory diseases;     -   hepatoprotective agents;     -   agents used in the treatment of heart failure or coronary         insufficiency Anti-hypertensive and hypotensive agents;     -   anti-coagulant, vasodilators;     -   anti-ischemic agents;     -   agents used in the treatment of metabolic diseases, such as         anti-diabetic, hypolipidemic, hypocholesterolemic,         anti-atherosclerotic and anti-obesity agents.     -   anti-viral agents;     -   anti-cancer agents and cancer prevention agents;     -   anti-cholestatic agents;     -   anti-fibrotic agents;     -   anti-NAFLD agents;     -   anti-NASH agents.

In a particular embodiment, the invention relates to the use of a compound of formula (I) or (Ia) in combination with an anti-fibrotic, anti-NAFLD or anti-NASH agent. Therefore, the invention relates to a first combination product comprising:

a) a RORgamma modulator, such as a compound of formula (I) or (Ia) or a pharmaceutically acceptable salt thereof; and

b) another therapeutically active agent.

In a particular embodiment, the other therapeutically active agent is an anti-fibrotic, anti-NAFLD or anti-NASH agent. In another particular embodiment, the other therapeutically active agent is a PPAR activator as defined below.

In a particular embodiment, the combination product is a composition comprising the RORgamma modulator and the other therapeutically active agent, and a pharmaceutically acceptable carrier.

In another embodiment, the combination product is a kit of parts comprising components a) and b) of the combination product. The kit of parts of the invention is for sequential, separate or simultaneous use in the treatment of any of the diseases mentioned above.

In another aspect, the invention relates to a combination of a RORγ modulator and a PPAR activator. In a particular embodiment, the invention relates to a composition comprising a RORγ modulator and a PPAR activator. In another embodiment, the invention relates to a kit-of-parts comprising a RORγ modulator and a PPAR activator, for simultanate, separate or sequential use.

The PPARs (α, β/δ (herein after δ), γ) belong to the hormone-activated nuclear receptor family. The PPARs, or “Peroxisome Proliferator Activated Receptors”, are nuclear receptors from the superfamily of transcription factors activated by the following ligands: steroids/thyroid hormones/retinoids. To date, three PPAR isotypes have been identified in mice and humans: PPARα, PPARδ and PPARγ. While PPARb/d expression in humans appears to be ubiquitous, PPARα and γ exhibit a differential tissue distribution (Braissant O and Wahli W, 1998). PPARa is expressed in cells with high fatty acid catabolic activity and in cells with high peroxisomal activity (hepatocytes, cardiomyocytes, renal proximal tubules, intestinal mucosa). PPARb/d is expressed ubiquitously and abundantly in most tissues. As far as PPARγ expression is concerned, it is limited mainly to adipose tissue, certain immune system cells and retina and is present in only trace amounts in other organs (Braissant O and Wahli W, 1998).

Taking the example of PPARα, its action is mediated by a class of compounds such as the fibrates which have a lipid-lowering effect. Natural ligands have also been identified such as for example fatty acids, eicosanoids (leukotriene B4) and 8(S)-hydroxyeicosatetraenoic acid (Kliewer S A et al., 1997). The PPARs have been associated primarily with lipid and glucose metabolism. PPAR activators, such as fibrates, enable a regulation of plasma cholesterol and triglyceride concentrations via activation of PPARα (Hourton D et al., 2001). Fibrate therapy leads to an increase in fatty acid oxidation in liver. Fibrates also decrease the synthesis of triglycerides (Staels B and Auwerx J, 1998). PPARα activators are also capable of correcting hyperglycemia and insulin level. Fibrates also reduce adipose tissue mass through a mechanism which is independent of food intake and leptin gene expression (Guerre-Millo M et al., 2000). The therapeutic interest of PPARγ agonists has been widely investigated in the treatment of type 2 diabetes (Spiegelman B M, 1998). It has been shown that PPARγ agonists restore insulin sensitivity in target tissues and reduce plasma glucose, lipid and insulin levels both in animal models of type 2 diabetes and in humans (Ram V J, 2003). PPAR activation by ligands also plays a role in regulating the expression of genes that participate in processes such as inflammation, angiogenesis, cell proliferation and differentiation, apoptosis and the activities of iNOS, MMPase and TIMPs. Activation of PPARα in keratinocytes results in a cessation of their proliferation and expression of genes involved in differentiation (Komuves L G et al., 2000). The PPARs have anti-inflammatory properties because they negatively interfere with transcription mechanisms involving other transcription factors like NF-κB or transcriptional activators like STAT and AP-1 (Desvergne B and Wahli W, 1999). Said anti-inflammatory and anti-proliferative properties make the PPARS (and particularly PPARα) interesting therapeutic targets for the treatment of diseases such as vascular occlusive diseases (atherosclerosis, etc.), hypertension, diseases related to neovascularization (diabetic retinopathy, etc.), inflammatory diseases (inflammatory bowel disease, psoriasis, etc.) and neoplastic diseases (carcinogenesis, etc.).

The combination of the invention may be used as a medicament. In a particular embodiment, the combination is used for the treatment of one of the diseases mentioned above. The RORγ modulator and the PPAR activator are each administered to a subject in need thereof in a therapeutically effective amount.

In a particular embodiment, the ROR modulator in the combination is a compound of formula (I) or (Ia).

In a particular embodiment, the PPAR activator in the combination is a PPARα, PPARγ, PPARγ, PPARα/δ (or dual PPARα/δ), PPARα/γ (or dual PPARα/γ), PPARγ/δ (or dual PPARγ/δ), or PPARα/γ/δ (or pan-PPAR) activator.

In a particular embodiment, the PPAR alpha agonist is a fibrate such as fenofibrate, ciprofibrate, pemafibrate, gemfibrozil, clofibrate, binifibrate, clinofibrate, clofibric acid, nicofibrate, pirifibrate, plafibride, ronifibrate, theofibrate, tocofibrate or SR10171.

In a particular embodiment, the PPAR gamma agonist is a glitazone (or thiazolidinedione) such as Rosiglitazone, Pioglitazone, deuterated pioglitazone, efatutazone, ATx08-001, OMS-405, CHS-131, THR-0921, SER-150-DN, KDT-501, GED-0507-34-Levo, CLC-3001 or ALL-4.

In a particular embodiment, the PPAR delta agonist is GW501516 (Endurabol or ({4-[({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)sulfanyl]-2-methylphenoxy}acetic acid)), MBX8025 (Seladelpar or {2-methyl-4-[5-methyl-2-(4-trifluoromethyl-phenyl)-2H-[1,2,3]triazol-4-ylmethylsylfanyl]-phenoxy}-acetic acid), GW0742 ([4-[[[2-[3-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolyl]methyl]thio]-2-methyl phenoxy]acetic acid), L165041, HPP-593 or NCP-1046.

In a particular embodiment, the PPAR alpha/gamma dual agonist is a glitazar such as Saroglitazar, Aleglitazar, Muraglitazar, Tesaglitazar or DSP-8658.

In a particular embodiment, the PPAR alpha/delta dual agonist is Elafibranor (GFT505) or T913659.

In a particular embodiment, the PPAR gamma/delta dual agonist is a conjugated linoleic acid (CLA) or T3D-959.

In a particular embodiment, the PPAR alpha/gamma/delta pan agonist is IVA337, TTA (tetradecylthioacetic acid), Bavachinin, GW4148, GW9135, Bezafibrate, Lobeglitazone or CS038.

In a more particular embodiment, the PPAR activator is a compound of formula (II), or a pharmaceutically acceptable salt thereof:

in which:

-   -   Y1 represents a halogen, a Ra, or Ga—Ra group;     -   A represents a CH═CH or a CH2-CH2 group;     -   Y2 represents a Gb-Rb group;     -   Ga and Gb, identical or different, represent an atom of oxygen         or sulfur;     -   Ra represents a hydrogen atom, an unsubstituted (C1-C6)alkyl         group, a (C6-C14)aryl group or a (C1-C6)alkyl group that is         substituted by one or more halogen atoms, a (C1-C6)alkoxy or a         (C1-C6)alkylthio group, (C3-C14)cycloalkyl groups,         (C3-C14)cycloalkylthio groups or heterocyclic groups;     -   Rb represents a (C1-C6)alkyl group substituted by at least a         —COORc group, wherein     -   Rc represents a hydrogen atom, or a (C1-C6)alkyl group that is         substituted or not by one or more halogen atoms,         (C3-C14)cycloalkyl groups, or heterocyclic groups; and     -   Y4 and Y5, identical or different, representing a (C1-C6)alkyl         group that is substituted or not by one or more halogen atoms,         (C3-C14)cycloalkyl groups or heterocyclic groups.

In a particular embodiment of the compound of formula (II):

Y1 represents a halogen, a Ra, or a Ga—Ra group;

A represents a CH═CH group;

Y2 represents a Gb-Rb group;

Ga and Gb, identical or different, represent an atom of oxygen or sulfur;

Ra represents a (C1-C6)alkyl or (C3-C14)cycloalkyl group, in particular a (C1-C7)alkyl or (C3-C14)cycloalkyl group substituted or not by one or more halogen atoms;

Rb represents a (C1-C6)alkyl group substituted by a —COOR3 group, wherein Rc represents a hydrogen atom or an alkyl group having from one to four carbon atoms; and

Y4 and Y5 independently represent a (C1-C4)alkyl group.

In a particular embodiment of the compound of formula (II):

Y1 represents a Ra or Ga—Ra group;

A represents a CH2-CH2 group;

Y2 represents a Gb-Rb group;

Ga represents an atom of oxygen or sulfur and Gb represents an atom of oxygen;

Ra represents a (C1-C6)alkyl or (C3-C7)cycloalkyl group;

Rb represents a (C1-C6)alkyl group substituted by at least a —COORc group, wherein Rc represents a hydrogen atom or (C1-C4)alkyl group; and

Y4 and Y5 independently represent a (C1-C4)alkyl group.

In a particular embodiment of the compound of formula (II):

Y1 represents a halogen atom or a Ra or Ga—Ra group;

A represents a CH2-CH2 group;

Y2 represents a Gb-Rb group;

Ga represents an atom of oxygen or sulfur and Gb represents an atom of oxygen;

Ra represents a (C1-C6)alkyl or (C3-C14)cycloalkyl group that is substituted by one or more halogen atoms;

Rb represents a (C1-C6)alkyl group substituted or not by one or more halogen atoms and substituted by at least a —COORc group, wherein Rc represents a hydrogen atom or a (C1-C4)alkyl group; and

Y4 and Y5 represent a (C1-C4)alkyl group.

In a particular embodiment of the compound of formula (II), Gb is an oxygen atom and Rb is (C1-C6)alkyl group substituted by a —COORc group, wherein Rc represents a hydrogen atom or an unsubstituted linear or branched (C1-C4)alkyl group.

In a particular embodiment of the compound of formula (II), Y1 is a (C1-C6)alkylthio group that comprises a (C1-C6)alkyl group that is linear or branched that is substituted or not by one or more halogen atoms.

In a particular embodiment, the compound of formula (II) is selected in the group consisting of 1-[4-methylthiophenyl]-3-[3,5-dimethyl-4-carboxydimethylmethyloxy phenyl]prop-2-en-1-one (Elafibranor or GFT505), 1-[4-methylthiophenyl]-3-[3,5-dimethyl-4-isopropyloxy carbonyldimethylmethyloxyphenyl]prop-2-en-1-one, 1-[4-methylthiophenyl]-3-[3,5-dimethyl-4-tertbutyloxycarbonyldimethylmethyloxyphenyl] prop-2-en-1-one, 1-[4-trifluoromethylphenyl]-3-[3,5-dimethyl-4-tertbutyloxycarbonyl dimethylmethyloxyphenyl]prop-2-en-1-one, 1-[4-trifluoromethylphenyl]-3-[3,5-dimethyl-4-carboxydimethylmethyloxyphenyl]prop-2-en-1-one, 1-[4-trifluoromethyl oxyphenyl]-3-[3,5-dimethyl-4-tertbutyloxycarbonyldimethylmethyloxy phenyl] prop-2-en-1-one, 1-[4-trifluoromethyloxyphenyl]-3-[3,5-dimethyl-4-carboxydimethylmethyl oxyphenyl]prop-2-en-1-one, 2-[2,6-dimethyl-4-[3-[4-(methylthio)phenyl]-3-oxo-propyl] phenoxy]-2-methylpropanoic acid, and 2-[2,6-dimethyl-4-[3-[4-(methylthio) phenyl]-3-oxo-propyl]phenoxy]-2-methyl-propanoic acid isopropyl ester.

In a more particular embodiment, the PPAR activator is 1-[4-methylthiophenyl]-3-[3,5-dimethyl-4-carboxydimethylmethyloxy phenyl]prop-2-en-1-one (or Elafibranor—GFT505), or a pharmaceutically acceptable salt thereof.

In a particular aspect, the invention relates to a combination product comprising:

i) a RORgamma modulator, in particular a compound of formula (I) or (Ia) or a pharmaceutically acceptable salt thereof;

ii) a PPAR activator, in particular a compound of formula (II) or a pharmaceutically acceptable salt thereof, in particular Elafibranor or a pharmaceutically acceptable salt thereof.

In a particular embodiment, the combination product is a composition comprising:

i) a RORgamma modulator, in particular a compound of formula (I) or (Ia) or a pharmaceutically acceptable salt thereof; and

ii) a PPAR activator, in particular a compound of formula (II) or a pharmaceutically acceptable salt thereof, in particular Elafibranor or a pharmaceutically acceptable salt thereof; and

iii) a pharmaceutically acceptable carrier.

In a particular embodiment, the combination product is a kit of parts comprising:

i) a RORgamma modulator, in particular a compound of formula (I) or (Ia) or a pharmaceutically acceptable salt thereof; and

ii) a PPAR activator, in particular a compound of formula (II) or a pharmaceutically acceptable salt thereof, in particular Elafibranor or a pharmaceutically acceptable salt thereof;

for sequential, separate or simultaneous use in the treatment of any of the diseases mentioned above.

Several other advantages of the invention will rise in the reading of the following examples; they should be considered as illustrative data and not as limitative ones.

EXAMPLES

Chemical names follow IUPAC nomenclature. Starting materials and solvents were purchased from commercial suppliers (Acros Organic, Sigma Aldrich, Combi-Blocks, Fluorochem, Fluka, Alfa Aesar or Lancaster) and were used as received without further purification. Some starting materials can be readily synthesized by a person skilled in the art. Air and moisture sensitive reactions were carried out under an inert atmosphere of nitrogen, and glassware was oven-dried. No attempts were made to optimize reaction yields. Thin-layer chromatography (TLC) was done on Merck silica gel 60 UV254 (250 μm) plates. Visualization was accomplished with UV light. Column chromatography was performed on Geduran silica gel 60 (40-63 μm) from Merck. Melting points (mp) were recorded with a Büchi Melting Point B-545 and are uncorrected. All microwave irradiation experiments were carried out in a Biotage Initiator microwave apparatus. ¹H spectra were recorded on Bruker Advance I spectrometer at 300 MHz. Chemical shifts (δ) are reported in ppm (parts per million), by reference to the hydrogenated residues of deuterated solvent as internal standard: 2.50 ppm for DMSO-d6, 7.26 ppm for CDCl3, and 3.31, and 4.78 for Methanol-d4. The spectral splitting patterns are designated as follows: s, singlet; d, doublet; dd, doublet of doublets; ddd, doublet of doublet of doublets; t, triplet; dt, doublet of triplets; q, quartet; m, multiplet; br s, broad singlet. Coupling constants (J) are quoted to the nearest 0.1 Hz. All tested compounds exhibited >95% chemical purity assessed by HPLC on a Merck HITACHI Lachrom L-7000 series and Merck HITACHI diode array detector L-7455 with a Waters column Symmetry C18 (3.5 μm, 4.6*75 mm) and using a gradient of MeOH/Millipore water containing 0.1% of formic acid. Chromatograms were analyzed with Lachrom software version 890-8800-09. Mass spectrometry measurements were performed on Alliance 2695 and DAD detector 2998 equiped with an Acquity QDa detector from Waters using a Waters column Symmetry C18 (3.5 μm, 4.6*75 mm) and using a gradient of MeOH/Millipore water containing 0.1% of formic acid (chromatograms were analyzed with Empower 3 software) or they were performed on apparatus equipped with Waters 2545 binary gradient module, Waters 2489 UV/Visible detector and Acquity QDa detector using a Waters column Symmetry C18 (3.5 μm, 4.6*75 mm) and using a gradient of MeOH/Millipore water containing 0.1% of formic acid (chromatograms were analyzed with MassLynx 4.1). Preparative HPLC were performed on apparatus equipped with Waters 2545 binary gradient module, Waters 2489 UV/Visible detector, Acquity QDa detector and Waters 2767 sample manager using a Waters column SymmetryPrep C18 (7 μm, 19*150 mm) and using a gradient of MeOH/Millipore water containing 0.1% of formic acid (chromatograms were analyzed with MassLynx 4.1). All solvents are HPLC grade.

The compounds of the invention are prepared according to the general methods and general protocols of synthesis given below. Representative procedures suitable for the preparation of compounds of formula (I) or (Ia) are outlined in the Reaction Schemes for intermediate (FIG. 1 and FIG. 2) and final (FIG. 3) compounds. Reagents and conditions may be adapted and additional steps employed to produce further compounds encompassed in the present invention having alternative substituent groups, or for achieving such compounds at higher yield and/or of higher purity.

Example 1: Synthesis of Intermediates for the Synthesis of Compounds According to the Invention

In the following, compounds termed “Ex. X” are intermediate compounds used for the synthesis of compounds of the present invention.

The general treatments and purification steps are carried out according to techniques well known by a person skilled in the art or such as those described in the literature: the reaction was quenched either with water, brine or sat. NH4Cl. Excess or solvent used for the reaction was removed under reduced pressure. The aqueous layer was extracted three times with a non-water miscible solvent (e.g. Et2O, EtOAc, CH2Cl2). The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. Purification of the crude material was realized either by double extraction using conc. HCl and NaOH 2N, by hydrochloride formation or by purification on silica gel column chromatography using standard mixture systems (cyclohexane/EtOAc, CH2Cl2/MeOH and CH2Cl2/EtOAc).

Example 1a: Synthesis of Acid Intermediates for the Synthesis of Compounds According to the Invention Intermediate Ex. 1: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetic acid (FIG. 1AA)

4-Aminophenylacetic acid (1.0 g, 6.62 mmol) was suspended in water (20 mL). Divinylsulfone (797 μL, 7.94 mmol), boric acid (123 mg, 1.99 mmol) and glycerol (146 μl, 1.99 mmol) were added and the mixture was heated to reflux for 4 h. The mixture was cooled to rt and stirred overnight to afford a suspension. EtOAc was added and the phases were mixed until all solid was dissolved. The organic phase was separated, the aqueous layer washed with EtOAc and the combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [95:5]. The residue was triturated with Et2O and then dried under vacuum at 60° C. to constant weight to afford 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetic acid (1.46 g, 82%) as yellow solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.11 (s, 4H), 3.46 (s, 2H) 3.74 (s, 4H), 6.97 (d, 2H, J=8.5 Hz), 7.14 (d, 2H, J=8.4 Hz).

Intermediate Ex. 3: 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid (FIG. 1AB)

TABLE 1.1 Starting compounds, Reaction conditions and purification, Cpd. Yield, appearance, ¹H NMR (solvent) data Ex.3a 2-(2-methyl-5-nitrophenyl)acetic acid Step 1: a solution of o-tolyacetic acid (5.0 g, 33.29 mmol), in CH2Cl2 (15 mL) was added dropwise to a pre-cooled mixture of conc. sulfuric acid (26 mL, 266.3 mmol) and 99.5% nitric acid (1.35 mL, 31.63 mmol) at −20° C. The reaction mixture was stirred at that temperature for 30 min, then slowly warmed to rt and stirred for 15 h. The reaction mixture was poured into ice-water. The white solid was collected by filtration and washed with water. The solid was triturated with Et2O and filtered to obtain the mono and di-nitration products in a 1:1 ratio (4.78 g), that will be separated after the next esterification step. Ex.3b methyl 2-(2-methyl-5-nitrophenyl)acetate Step 2: 4 M HCl in dioxane (26.6 mL, 106.46 mmol)) was added to a solution of previously synthesized nitro derivative Ex.3a (10.39 g, 53.23 mmol) in methanol (150 mL). The reaction mixture was refluxed for 15 h. After cooling to rt and removing the excess of solvent under reduced pressure, the crude product was dissolved in water and basified to pH > 12 using 2N NaOH. The aqueous layer was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, filtered and the solution was concentrated to reduced pressure. The residue was purified by flash chromatography on silica gel eluting with heptanes and EtOAc to afford methyl 2-(2-methyl-5-nitrophenyl)acetate Ex.3b (2.55 g, 23%). Ex.3c methyl 2-(5-amino-2-methylphenyl)acetate Step 3: methyl 2-(2-methyl-5-nitrophenyl)acetate Ex.3b (2.55 g, 12.19 mmol) was dissolved in ethanol (60 mL). To this solution was added 10% palladium on carbon (ca 260 mg). The mixture was degassed with N2 and a balloon filled with hydrogen was fitted. The reaction was stirred at rt for 2 h. The reaction mixture was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure and dried under high vacuum to afford the desired product in a high purity grade (2.10 g, 96%). Ex.3d methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetate Step 4: water (20 mL), boric acid (220 mg, 3.52 mmol) and cat. glycerol (few drops) were added to a solution of methyl 2-(5-amino-2-methylphenyl)acetate Ex.3c (2.10 g, 11.72 mmol) and divinyl sulfone (1.18 mL, 11.72 mmol). The resulting mixture was stirred under reflux for 5 h. The reaction mixture was extracted with EtOAc and the organic layer was washed with water and brine, dried over MgSO4, filtered and the solvent was evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with heptanes and EtOAc affording methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- methylphenyl]acetate Ex.3d (3.15 g, 90%). Ex.3 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid Step 5: methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetate Ex.3d (3.15 g, 10.59 mmol) was dissolved in THF—H2O (4:1, 24 mL/6 mL) and lithium hydroxide monohydrate (1.33 g, 31.77 mmol) was added at 0° C. Then, the reaction mixture was allowed to warm up to rt and stirred for 15 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water, pH adjusted to 4-5 and the product was extracted with CH2Cl2. The combined organic extracts were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The resulting solid was triturated in Et2O and then filtered to afford 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- methylphenyl]acetic acid Ex.3 (1.06 g, 35%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 2.14 (s, 3H), 3.11 (s, 4H), 3.53 (s, 2H), 3.70 (s, 4H), 6.82 (d, 1H), 6.88 (s, 1H), 7.04 (m, 1H), 12.28 (br(s), 1H).

Intermediate Ex. 4: 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetic acid (FIG. 1AC)

TABLE 1.2 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.4a Methyl 2-fluoro-5-nitrophenyl acetate Step 1: 2-fluoro-5-nitrophenyl acetic acid (10 g, 50.22 mmol) was dissolved in MeOH (200 mL). 4 M HCl in dioxane (20 mL) was added and the mixture was heated to 50° C. for 16 h. The reaction mixture was cooled to rt and concentrated to dryness to afford a pale brown oil. No purification was carried out. The product (10.6 g) was transferred into the next step. Ex.4b methyl 2-(5-amino-2-fluorophenyl)acetate Step 2: methyl 2-(2-fluoro-5-nitrophenyl)acetate Ex.4a (10.6 g, 49.7 mmol) was dissolved in MeOH (200 mL). The mixture was purged with nitrogen. A catalytic amount of Pd/C (10%) was added under nitrogen atmosphere. The nitrogen atmosphere was replaced by hydrogen and the mixture was stirred for 16 h at rt. Hydrogenation was continued for 60 h. The mixture was filtered through a pad of Celite and washed with MeOH. The filtrate was concentrated to dryness to afford a yellow oil. The crude material was purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [70:30]. The product fractions were combined and concentrated to dryness to afford methyl 2- (5-amino-2-fluorophenyl)acetate Ex.4b (8.11 g, 89%) as pale brown oil. Ex.4c methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetate Step 3: methyl 2-(5-amino-2-fluorophenyl)acetate Ex.4b (1.0 g, 5.46 mmol) was suspended in water (20 mL). Divinyl sulfone (659 μL, 6.55 mmol), boric acid (101 mg, 1.64 mmol) and glycerol (121 μL, 1.64 mmol) were added and the mixture was heated to reflux for 16 h. The two phase mixture was cooled to rt, EtOAc was added and the phases where separated. The organic layer was concentrated to dryness to afford a brown oil. The crude was purified by column chromatography eluting with heptane and a gradient of heptane/CH2Cl2 from [100:0] to [1:1]. The product fractions were combined and concentrated to dryness to afford methyl 2- [5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetate Ex.4c (1.70 g, quantitative) as pale yellow oil. Ex.4 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetic acid Step 4: methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetate Ex.4c (1.70 g, 5.64 mmol) was dissolved in THF/H2O (4:1, 20 mL/5 mL). Lithium hydroxide monohydrate (355 mg, 8.46 mmol) was added and the mixture was stirred at rt for 16 h. Further lithium hydroxide monohydrate (0.5 equiv) was added and stirring at rt was continued. The reaction mixture was quenched with EtOAc and water. 2 N HCl was added under vigorous stirring until pH 4-5 was reached. The two phases were separated. The aqueous layer was extracted several times with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness to afford a yellow oil. The oil was passed through a pad of silica eluting with CH2Cl2/MeOH [9:1]. The product fractions were combined and concentrated to dryness to afford a colourless oil which solidified upon standing at rt. Some MeOH was added and the solid was collected by filtration. The product was dried to constant weight under vacuum at 60° C. to afford 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]acetic acid Ex.4 (706 mg, 44%) as white solid. The filtrate was concentrated to dryness to afford a less pure second crop of title compound (720 mg) which was not further purified. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.06-3.08 (m, 4H), 3.49 (s, 2H), 3.59- 3.61 (m, 4H), 6.85-7.01 (m, 3H), 12.35 (br (s), 1H).

Intermediate Ex. 7: 2-[2-fluoro-5-(morpholin-4-yl)phenyl]acetic acid (FIG. 1AD)

TABLE 1.3 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.7a methyl 2-(5-bromo-2-fluorophenyl)acetate Step 1: 5-bromo-2-fluoro-phenylacetic acid (5.0 g, 21.46 mmol) was dissolved in MeOH (150 mL). 4 M HCl in dioxane (20 mL) was added and the mixture was heated to 50° C. for 16 h. The mixture was concentrated to dryness to afford a yellow oil. The oil was passed through a pad of silica with heptane/EtOAc [1:1]. The product fractions were combined and concentrated to dryness to afford methyl 2-(5-bromo-2-fluorophenyl)acetate Ex.7a (5.01 g, 95%) as colourless oil. Ex.7b 2-(2-fluoro-5-morpholinophenyl)acetate Step 2: methyl 2-(5-bromo-2-fluorophenyl)acetate Ex.7a (600 mg, 2.43 mmol) was dissolved in dry toluene (20 mL). The mixture was purged with nitrogen. Morpholine (528 μL, 6.07 mmol), K3PO4 (1.29 g, 6.07 mmol), Pd2(dba)3 (114 mg, 0.12 mmol) and DavePhos (96 mg, 0.25 mmol) were added the mixture was heated to 90° C. for 16 h. After 16 h, the reaction mixture was cooled to rt, diluted with EtOAc and washed with water. The organic layer was concentrated to dryness and purified by column chromatography eluting with heptane and a gradient of heptane/ EtOAc from [100:0] to [75:25]. The product fractions were combined and concentrated to dryness to afford methyl 2-(2-fluoro- 5-morpholinophenyl)acetate Ex.7b (345 mg, 56%) as pale yellow oil. Ex.7 2-[2-fluoro-5-(morpholin-4-yl)phenyl]acetic acid Step 3: methyl 2-(2-fluoro-5-morpholinophenyl)acetate Ex.7b (345 mg, 1.36 mmol) was dissolved in THF/H2O (4:1, 10 mL/2 mL). Lithium hydroxide monohydrate (172 mg, 4.09 mmol) was added and the mixture was stirred at rt for 60 h. The mixture was diluted with EtOAc and 1 N HCl was added under vigorous stirring until pH 3-4 was reached. The phases were separated, the organic layer was concentrated to dryness to afford a yellow oil. The crude material was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [95:5]. The product fractions were combined and concentrated to dryness to afford a pale pink oil. Et2O was added and a pale pink solid was formed. The solvent was evaporated and the product dried under vacuum to constant weight to afford 2-[2-fluoro-5-(morpholin-4-yl) phenyl]acetic acid Ex.7 (201 mg, 62%) as pale pink solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.02 (m, 4H), 3.56 (s, 2H), 3.71-3.74 (m, 4H), 6.82-6.92 (m, 2H), 7.00-7.06 (m, 1H), 12.40 (br(s), 1H).

Intermediate Ex. 10: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid (FIG. 1AE)

TABLE 1.4 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.10a 2-(4-amino-3-methyl-phenyl)acetic acid Step 1: 2-(3-methyl-4-nitro-phenyl)acetic acid (1.5 g, 7.69 mmol) was dissolved in MeOH (30 mL). The solution was purged with nitrogen and Pd/C (5%) (150 mg) was added under nitrogen atmosphere. The nitrogen atmosphere was replaced by hydrogen and the mixture was stirred at rt and monitored by TLC. Additional MeOH was added to the mixture and the catalyst was removed by filtration through a pad of Celite. The catalyst was washed with DMF, MeOH and CH2Cl2 and the filtrate was concentrated to dryness to afford a brown oil. No purification was carried out. The product (3.0 g) was used as such in the next synthetic step. Ex.10 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid Step 2: 2-(4-amino-3-methylphenyl)acetic acid Ex.10a (1.27 g, 7.69 mmol) was suspended in water (30 mL). Divinyl sulfone (926 μL, 9.22 mmol), boric acid (143 mg, 2.31 mmol) and glycerol (170 μL, 2.31 mmol) were added and the mixture was heated to reflux for 1 h. The reaction mixture was cooled to rt and extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness to afford a dark yellow sticky solid. The solid was adsorbed onto silica gel and was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [95:10]. The product fractions were combined and concentrated to dryness to afford an off white solid. The solid was triturated with Et2O, filtered and then dried under vacuum at 60° C. to constant weight to afford 2-[4-(1,1- dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid Ex.10 (718 mg, 33%) as white solid. A second crop (620 mg) was isolated (less pure material). 1H NMR (300 MHz, DMSO-d6, δ in ppm): 2.29 (s, 3H), 3.29 (s, 8H), 3.50 (s, 2H), 7.04-7.10 (m, 3H), 12.28 (br(s), 1H).

Intermediate Ex. 17: 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetic acid (FIG. 1AF)

TABLE 1.5 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.17a tert-butyl 2-(bromozincio)acetate Step 1: to a solution of Zn dust (3.0 g, 317b0.26 mL) in dry THF (25 mL) at rt was added 1,2-dibromoethane (434 μL, 5.04 mmol) under atmosphere of nitrogen. The reaction mixture was stirred at 70° C. for 1 min and cooled down to rt. This procedure was repeated 3 times. Me3SiCl (256 μL, 2.02 mmol) was added and the resulting suspension was stirred at rt for 15 min. It was then heated to 65° C. and a few drops of tert-butyl 2-bromoacetate were added. Then a solution of tert-butyl 2-bromoacetate (4.92 g, 25.22 mmol) in dry THF (5 mL) was added at such a rate that reflux was maintained. Upon completion of addition, the reaction mixture was refluxed for an additional 20 min and allowed to cool down to rt The zinc was allowed to settle and the supernatant was used further without any analysis. Complete conversion was assumed. Ex.17b 4-(5-bromopyrimidin-2-yl)-1-thiomorpholine-1,1-dione Step 2: DIPEA (1.33 mL, 7.74 mmol), was added to 5-bromo-2-chloropyrimidine (1.0 g, 5.16 mmol) in CH3CN (20 mL). Then, thiomorpholine-1,1-dioxide (697 mg, 5.16 mmol) was added to the mixture. The reaction mixture was heated at 50° C. for 72 h. The solvent was concentrated to dryness to afford an oil. Water and EtOAc were added to the crude. The organic layer was separated, concentrated to dryness to afford an oil. The crude material was purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness to afford 4-(5-bromopyrimidin-2-yl)-1-thiomorpholine-1,1-dione Ex.17b (935 mg, 62%) as white solid. Ex.17c tert-butyl 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetate Step 3: 4-(5-bromopyrimidin-2-yl)-1-thiomorpholine-1,1-dione Ex.17b (935 mg, 3.20 mmol), the freshly prepared tert-butyl 2-(bromozincio)acetate Ex.17a (11.3 mL, 9.60 mmol) and dry THF (10 mL) were charged to flask, the mixture was purged with nitrogen for 5 min. Then, XPhos (305 mg, 0.64 mmol) and Pd2(dba)3 (293 mg, 0.32 mmol) were added and the reaction mixture was stirred at 75° C. for 16 h. EtOAc was added and the phases were separated, the organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The desired fractions were combined and concentrated to obtain tert- butyl 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetate Ex.17c (984 mg, 94%) as yellow oil. Ex.17 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetic acid Step 4: 4 M HCl in dioxane (3 mL, 12 mmol) was added to tert-butyl 2-[2-(1,1- dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetate Ex.17c (984 mg, 3.00 mmol). The reaction mixture was stirring for 16 h at rt. A solid (salt) was formed, it was collected by filtration, washed with Et2O and dried under vacuum until constant weight to give 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetic acid Ex.17 (834 mg, 82%) as pale yellow solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.14 (br(s), 4H), 3.50 (s, 2H), 4.20 (br(s), 4H), 8.35 (s, 2H).

Intermediate Ex. 19: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid (FIG. 1AG)

2-(4-Amino-2-methylphenyl)acetic acid (1.0 g, 6.05 mmol) was suspended in water (20 mL). Divinyl sulfone (729 μL, 7.26 mmol), boric acid (112 mg, 1.82 mmol) and glycerol (133 μL, 1.82 mmol) were added and the mixture was heated to reflux for 2 h. The mixture was cooled to rt and stirred overnight. The mixture was extracted with EtOAc and the combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [95:5]. The product fractions were combined and concentrated to dryness to afford an off pale yellow solid. The solid was triturated with Et2O, filtered and then dried under vacuum at 60° C. to constant weight yielding 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetic acid Ex. 19 (1.214 g, 71%) as pale yellow solid.

1H NMR (300 MHz, DMSO-d6, δ in ppm): 2.20 (s, 3H), 3.10 (br(s), 4H), 3.47 (s, 2H), 3.73 (m, 4H), 6.79 (d, 1H, J=8.3 Hz), 6.85 (s, 1H), 7.05 (d, 1H, J=8.3 Hz), 12.19 (s, 1H).

Intermediate Ex. 22: 2-[6-(morpholin-4-yl)pyridin-3-yl]acetic acid (FIG. 1AH)

TABLE 1.6 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 22a methyl 2-(6-fluoropyridin-3-yl)acetate Step 1: 5-bromo-2-fluoropyridine (2.92 mL, 28.41 mmol), methyl acetoacetate(9.20 mL, 85.23 mmol) and K3PO4 (24.122 g, 113.64 mmol) were charged to a flask, toluene (280 mL) was added and the mixture was purged with nitrogen for 5 min. Then Pd(OAc)2 (318 mg, 1.42 mmol) and tBuXPhos (1.21 g, 2.85 mmol) were added and the reaction mixture was stirred at 120° C. for 20 h. The reaction mixture was quenched with EtOAc and water. After phase separation the organic layer was washed with brine, dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude was purified by flash column chromatography on silica gel eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [85:15]. The desired fractions were combined and concentrated to afford methyl 2-(6-fluoropyridin-3-yl)acetate Ex. 22a (1.7 g, 35%) as off-white oil. Ex. 22b methyl 2-(6-morpholinopyridin-3-yl)acetate Step 2: methyl 2-(6-fluoropyridin-3-yl)acetate Ex. 22a (0.5 g, 2.96 mmol) was dissolved in toluene and morpholine (2.6 mL, 29.55 mmol) was added. The reaction mixture was heated to 120° C. for 48 h. The reaction mixture was cooled to rt and quenched with EtOAc and water. After phases separation the organic layer was washed with brine, dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [70:30]. The desired fractions were combined and concentrated to afford methyl 2-(6-morpholinopyridin-3-yl)acetate Ex. 22b (290 mg, 42%) as yellow oil. Ex. 22 2-(6-morpholinopyridin-3-yl)acetic acid hydrochloride Step 3: methyl 2-(6-morpholinopyridin-3-yl)acetate Ex. 22b (290 mg, 1.22 mmol) was dissolved in THF/H2O (5:1, 10 mL/2.5 mL). Lithium hydroxide monohydrate (101 mg, 2.44 mmol) was added and the mixture was stirred at rt for 16 h. THF was removed under vacuum. EtOAc and water were added followed by 1N HCl under vigorous stirring until pH 4 was reached. The phases were separated. However, the desired product was observed in both phases. Both phases were joined and adsorbed on silica gel. The resulting crude was purified by column chromatography eluting CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [75:25]. The product fractions were combined and concentrated to dryness to afford a yellow oil. HCl/dioxane was added to form the corresponding salt. The supernatant was removed and the solid was dried under vacuum to constant weight to afford 2-(6-morpholinopyridin-3- yl)acetic acid hydrochloride Ex. 22 (217 mg, 80%) as off-white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.46-3.60 (m, 6H), 3.70-375 (m, 4H), 6.92 (m, 1H), 7.57 (m, 1H), 8.02 (s, 1H), 12.47 (br(s), 1H).

Intermediate Ex. 23: 2-[2-(morpholin-4-yl)pyrimidin-5-yl]acetic acid (FIG. 1AI)

TABLE 1.7 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 23a 5-bromo-2-morpholinopyrimidine Step 1: DIPEA (640 μL, 3.87 mmol) was added to 5-bromo-2-chloropyrimidine (500 mg, 2.58 mmol) in CH3CN (11 mL). Then, morpholine (220 mg, 2.58 mmol) was added to the mixture. The reaction mixture was stirred at rt for 16 h. The solvent was evaporated to dryness and water followed by CH2Cl2 were added to the crude material. The organic layer was separated and concentrated to dryness. The residue was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [9:1]. The product fractions were combined and concentrated to dryness to afford 5-bromo-2- morpholinopyrimidine Ex. 23a (535 mg, 85%) as white solid. Ex. 23b tert-butyl 2-(2-morpholinopyrimidin-5-yl)acetate Step 2: 5-bromo-2-morpholinopyrimidine Ex. 23a (535 mg, 2.19 mmol), freshly prepared tert-butyl 2-(bromozincio)acetate Ex. 17a (7 mL) and dry THF (6 mL) were placed in a flask. The mixture was purged with nitrogen for approx. 5 min. Then Pd2(dba)3 (201 mg, 0.22 mmol) and XPhos (210 mg, 0.44 mmol) were added and the reaction mixture was stirred at 75° C. for 16 h. The reaction mixture was concentrated and the residue was diluted with EtOAc and water. After phase separation, the combined organic layers were washed with brine, dried over MgSO4, filtered and the solution was concentrated to dryness. The residue was purified by flash chromatography on silica eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The desired fractions were combined and concentrated to obtain tert-butyl 2-(2-morpholinopyrimidin-5- yl)acetate Ex. 23b (690 mg, quantitative) as colourless oil. Ex. 23 2-(2-morpholinopyrimidin-5-yl)acetic acid hydrochloride Step 3: 4M HCl in dioxane (3.58 mL, 14.32 mmol) was added to tert-butyl 2-(2- morpholinopyrimidin-5-yl)acetate Ex. 23b (1 g, 3.58 mmol) diluted in CH2Cl2 (2 mL). The reaction mixture was stirring for 16 h at rt. Further 4M HCl in dioxane (1 equiv) was added to the reaction mixture. The volatiles was removed under vacuum. The solid was triturated with Et2O and collected by filtration, washed with Et2O and dried under vacuum at constant weight to afford 2-(2- morpholinopyrimidin-5-yl)acetic acid hydrochloride Ex.23 (474 mg, 60%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.48 (s, 2H), 3.67 (s, 8H), 8.30 (s, 2H).

Intermediate Ex. 24: 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetic acid (FIG. 1AJ)

TABLE 1.8 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 24a 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetate Step 1: methyl 2-(6-fluoropyridin-3-yl)acetate Ex. 22a (400 mg, 2.36 mmol) was dissolved in toluene (1 mL) and thiomorpholine-1,1-dioxide (959 mg, 7.09 mmol) was added. The reaction mixture was heated at 120° C. for 48 h. The reaction mixture was diluted with EtOAc and water. After phase separation, the combined organic layers were washed with brine, dried over MgSO4, filtered and the solution was concentrated to dryness. The residue was purified by flash column chromatography on silica gel eluting with a gradient of heptane/EtOAc from [100:0] to [0:100]. The desired fractions were combined and concentrated to afford methyl 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetate Ex. 24a (255 mg, 38%) as yellow solid. Ex. 24 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetic acid Step 2: methyl 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetate (255 mg, 0.90 mmol) Ex. 24a was dissolved in THF/H2O (4:1, 8 mL/2 mL). Lithium hydroxide monohydrate (75 mg, 1.79 mmol) was added and the mixture was stirred at rt for 16 h. THF was removed under vacuum. EtOAc and water were added followed by 1M HCl under vigorous stirring until pH 4 was reached. The phases were separated. However, was observed desired product in both phases. Both phases were joined and absorbed onto silica gel. The crude was purified by column chromatography eluting CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [90:10]. The product fractions were combined and concentrated to dryness to afford a white solid. The resultant solid was triturated and washed with diethyl ether and dried under high vacuum to constant weight to give 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]acetic acid Ex. 24 (144 mg, 59%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.08 (br(s), 4H), 3.47 (s, 2H), 4.04 (br(s), 4H), 6.99 (m, 1H), 7.51 (m, 1H), 8.03 (m, 1H).

Intermediate Ex. 26: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]acetic acid (FIG. 1AK)

TABLE 1.9 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 26a 2-(4-amino-3-methoxyphenyl)acetic acid Step 1: Pd/C (10%) (100 mg) was added to a solution of 2-(3-methoxy-4- nitrophenyl)acetic acid (1.0 g, 4.7 mmol) in MeOH (5 mL) at rt. Then hydrogen was filled and the reaction mixture was stirred for 12 h. The solution was filtered through a pad of Celite and the filtrate was concentrated under vacuum to afford the product (849 mg, 99%). The residue was used in the next step without further purification. Ex. 26 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]acetic acid Step 2: 2-(4-amino-3-methoxyphenyl)acetic acid Ex. 26a (500 mg, 2.6 mmol) was suspended in water (2.5 mL). Divinyl sulfone (313 μL, 3.12 mmol), boric acid (96 mg, 1.56 mmol) and glycerol (215 mg, 2.34 mmol) were added and the mixture was heated to 13° C. overnight. The mixture was cooled to rt. CH2Cl2 was added and the phases were mixed until all solid was dissolved. The organic phase was separated, the aqueous layer washed with CH2Cl2 and the combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness. The product was triturated in Et20 and filtered-off to afford 2-[4-(1,1- dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]acetic acid Ex. 26 (198 mg, 28%) as pale red solid. 1H NMR (300 MHz, CDCl3, δ in ppm): 3.22 (br(s), 4H), 3.57 (br(s), 4H), 3.63 (s, 2H), 3.89 (s, 3H), 6.83-6.86 (m, 2H), 6.92 (d, 1H, J = 7.8 Hz).

Intermediate Ex. 27: 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]acetic acid (FIG. 1AL)

TABLE 1.10 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 27a 2-(3-amino-4-methoxyphenyl)acetic acid Step 1: Pd/C (10%) (100 mg) was added to a solution of 2-(4-methoxy-3- nitrophenyl)acetic acid (1.0 g, 4.7 mmol) in MeOH (5 mL) at rt. Then hydrogen was filled and the reaction mixture was stirred for 12 h. The solution was filtered through a pad of Celite and the filtrate was concentrated under vacuum to afford the product (803 mg, 94%). The residue was used in the next step without further purification Ex. 27 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]acetic acid Step 2: 2-(3-amino-4-methoxyphenyl)acetic acid Ex. 27a (500 mg, 2.6 mmol) was suspended in water (2.5 mL). Divinyl sulfone (313 μL, 3.12 mmol), boric acid (96 mg, 1.56 mmol) and glycerol (215 mg, 2.34 mmol) were added and the mixture was heated to 130° C. overnight. The mixture was cooled to rt. CH2Cl2 was added and the phases were mixed until all solid was dissolved. The organic phase was separated, the aqueous layer washed with CH2Cl2 and the combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness. The product was triturated in Et20 and filtered-off to afford 2-[3-(1,1- dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]acetic acid Ex. 27 (241 mg, 31%) as white solid. 1H NMR (300 MHz, CDCl3, δ in ppm): 3.15-3.27 (m, 4H), 3.57 (s, 2H), 3.60 (s, 4H), 3.88 (s, 3H), 6.85 (m, 2H), 6.99 (d, 1H, J = 8.3 Hz).

Intermediate Ex. 28: 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid (FIG. 1AM)

TABLE 1.11 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 28a methyl 1-(4-chlorophenyl)cyclopropanecarboxylate Step 1: 1-(4-chlorophenyl)-1-cyclopropanecarboxylic acid (600 mg, 3.05 mmol) was dissolved in MeOH (15 mL) to afford a clear colourless solution. 4M HCl in dioxane (2.5 mL) was added and the mixture was heated to 50° C. for 20 h. The reaction mixture was concentrated to dryness. EtOAc and sat. NaHCO3 solution was added and the two phases were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to reduced pressure. The residue was purified by column chromatography eluting with heptane and a gradient of heptane/EtAOc from [100:0] to [85:15]. The product fractions were combined and concentrated to dryness to afford methyl 1-(4- chlorophenyl)cyclopropanecarboxylate Ex. 28a (570 mg, 89%) as colourless oil. Ex. 28 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Step 2: methyl 1-(4-chlorophenyl)cyclopropanecarboxylate Ex. 28a (500 mg, 2.37 mmol) was dissolved with dry toluene (20 mL) and few amount of tBuOH. The mixture was purged with nitrogen. Thiomorpholine 1,1 dioxide (802 mg, 5.93 mmol), NaOtBu (570 mg, 5.93 mmol), Pd(OAc)2 (27 mg, 0.12 mmol) and XPhos (113 mg, 0.24 mmol) were added and it was closed under nitrogen atmosphere. The mixture was heated to 120° C. for 20 h. The reaction mixture was cooled to rt. EtOAc and water were added followed by 1N HCl under vigorous stirring until pH 4 was reached. The phases were separated. The organic layer was dried, filtered and the solution was concentrated to dryness. The crude material was absorbed on silica gel and purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [90:10]. The product fractions were combined and concentrated to dryness to afford a solid. The resultant solid was triturated and washed with Et2O and dried under high vacuum to afford 1-[4-(1,1-dioxo-1-thiomorpholin-4- yl)phenyl]cyclopropane-1-carboxylic acid Ex. 28 (397 mg, 57%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 1.07 (m, 2H), 1.40 (m, 2H), 3.11 (br(s), 4H), 3.74 (br(s), 4H), 6.93 (d, 2H, J = 8.5 Hz), 7.18 (d, 2H, J = 8.5 Hz).

Intermediate Ex. 29: 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid (FIG. 1AN)

TABLE 1.12 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 29a methyl 1-phenylcyclopropanecarboxylate Step 1: 1-phenyl-1-cyclopropanecarboxylic acid (10.0 g, 61.66 mmol) was dissolved in MeOH (150 mL). 4M HCl in dioxane (10 mL) was added and the mixture was heated to 50° C. for 20 h. The reaction mixture was concentrated to dryness. EtOAc and sat. NaHCO3 solution was added and the two phases were partitionated. The organic layer was dried over MgSO4, filtered and the solution concentrated to dryness to afford methyl 1-phenylcyclopropanecarboxylate Ex. 29a (10.55 g, 97%) as colourless oil. The compound was pure enough and used in the next step without further purification. Ex. 29b methyl 1-(4-nitrophenyl)cyclopropanecarboxylate Step 2: methyl 1-phenylcyclopropanecarboxylate Ex. 29a (10.55 g, 59.86 mmol) was dissolved in a mixture of conc. H2SO4 (25 mL) and CH2Cl2 (25 mL) and cooled to 0° C. KNO3 (6.05 g, 59.86 mmol) was added portionwise. The reaction mixture was stirred at 0° C. for 2 h and then allowed to warm up to rt. After 22 h, the mixture was diluted with EtOAc and water. The phases were separated, the organic layer was washed with sat. NaHCO3 solution, dried over MgSO4, filtered and the solution was concentrated to dryness. The residue was purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [30:70]. The product fractions were combined and concentrated to dryness to afford methyl 1-(4- nitrophenyl)cyclopropanecarboxylate Ex. 29b (7.93 g, 60%) as colourless oil, which solidified upon standing at rt Ex. 29c methyl 1-(4-aminophenyl)cyclopropanecarboxylate Step 3: methyl 1-(4-nitrophenyl)cyclopropanecarboxylate Ex. 29b (7.93 g, 35.85 mmol) was dissolved in MeOH (100 mL). The solution was purged with nitrogen and Pd/C (10%) (793 mg) was added under nitrogen atmosphere. The nitrogen atmosphere was replaced by hydrogen (balloon) and the mixture was stirred at rt for 20 h. The catalyst was removed by filtration, the filtrate was concentrated to dryness and purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [60:40]. The product fractions were combined and concentrated to dryness to afford methyl 1-(4- aminophenyl)cyclopropanecarboxylate Ex. 29c (5.13 g, 75%) as off-white solid. Ex. 29d methyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylate Step 4: methyl 1-(4-aminophenyl)cyclopropanecarboxylate Ex. 29c (5.13 g, 26.81 mmol) was dissolved in CH3CN (100 mL). N-bromosuccinimide (4.77 g, 26.81 mmol) was added and the mixture was stirred at rt for 20 h. The reaction mixture was concentrated to dryness. The residue was partitioned between water and EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness. The residue was purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [70:30]. The product fraction were combined and concentrated to dryness to afford methyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylate Ex. 29d (6.08 g, 84%) as pale brown sticky oil which solidified upon standing at rt. Ex. 29e methyl 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1- carboxylate Step 5: methyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylate Ex. 29d (500 mg, 1.85 mmol) was suspended in water (2.5 mL). Divinyl sulfone (225 μL, 2.22 mmol), boric acid (69 mg, 1.11 mmol) and glycerol (123 μL, 1.67 mmol) were added and the mixture was heated to reflux for 48 h. The mixture was cooled to rt. EtOAc was added and the phases were mixed until all solid was dissolved. The organic phase was separated, the aqueous layer washed with EtOAc and the combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The residue was purified by column chromatography eluting with heptane/EtAOc from [100:0] to [20:80]. The product fractions were combined and concentrated to afford methyl 1-[3-bromo-4-(1,1- dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylate Ex. 29e (340 mg, 47%). Ex. 29 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1- carboxylic acid Step 6: methyl 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4- yl)phenyl]cyclopropane-1-carboxylate Ex. 29e (340 mg, 0.88 mmol) was dissolved in THF/H2O (4:1, 8 mL/2 mL). Lithium hydroxide monohydrate (73 mg, 1.75 mmol) was added and the reaction mixture was stirred at rt for 16 h. Additional litthium hydroxide monohydrate (1.0 equiv) was added and the mixture was stirred at rt for 20 h. THF was removed under vacuum. EtOAc and water were added followed by 1N HCl under vigorous stirring until pH 4 was reached. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The resultant solid was triturated in Et2O and the precipitate was filtered-off to afford 1-[3-bromo-4-(1,1- dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 29 (233 mg, 71%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 1.13 (br(s), 2H), 1.43 (br(s), 2H), 3.25-3.55 (m, 8H), 7.20 (d, 1H, J = 8.2 Hz), 7.29 (d, 1H, J = 8.2 Hz), 7.55 (s, 1H)

Intermediate Ex. 30: 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetic acid (FIG. 1AO)

TABLE 1.13 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 30a 4-(5-bromo-4-methylpyrimidin-2-yl)-1-thiomorpholine-1,1-dione Step 1: DIPEA (804 μL, 4.70 mmol) was added to 5-bromo-2-chloro-4- methylpyrimidine (650 mg, 3.13 mmol) dissolved in CH3CN (20 mL). Then, thiomorpholine-1,1-dioxide (508 mg, 3.76 mmol) was added to the mixture. The mixture reaction was heated at 75° C. for 48 h. Solvent was removed under reduced pressure. H2O and AcOEt were added to the residue. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness to afford 4-(5-bromo-4-methylpyrimidin-2-yl)-1- thiomorpholine-1,1-dione Ex. 30a (732 mg, 76%) as yellow solid. The compound was used as such in the next step. Ex. 30b methyl 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]-3- oxobutanoate Step 2: 4-(5-bromo-4-methylpyrimidin-2-yl)-1-thiomorpholine-1,1-dione Ex. 30a (561 mg, 1.83 mmol), methyl acetoacetate (593 μL, 5.50 mmol) and K3PO4 (1.56 g, 7.33 mmol) were charged to a screw cap tube, toluene (25 mL) was added and the mixture was purged with nitrogen for 5 min. Then Pd(OAc)2 (20 mg, 0.09 mmol) and tBuXPhos (77 mg, 0.18 mmol) were added and the tube was closed under nitrogen atmosphere. The reaction mixture was stirred at 120° C. for 32 h. The reaction mixture was diluted with EtOAc and water. After phase separation, the combined organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [40:60]. The product fractions were combined and concentrated to dryness to afford methyl 2-[2-(1,1-dioxo-1- thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetate Ex. 30b (121 mg, 22%) as yellow solid. Likewise, intermediate methyl 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)- 4-methylpyrimidin-5-yl]-3-oxobutanoate was recovered (315 mg). Ex. 30 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetic acid hydrochloride Step 3: methyl 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5- yl]acetate Ex. 30b (246 mg, 0.82 mmol) was dissolved in THF/H2O (3:1, 12 mL/ 4 mL). Lithium hydroxide monohydrate (69 mg, 1.64 mmol) was added and the mixture was stirred at rt for 20 h. 1N HCl was added under stirring until pH 4 was reached. Then, the crude material was directly concentrated to dryness. The residue was triturated in Et2O and dried under high vacuum to afford 2-[2- (1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetic acid hydrochloride Ex. 30 (275 mg, crude) as an off-white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 2.29 (s, 3H), 3.11 (br(s), 4H), 3.26 (s, 2H), 4.19 (br(s), 4H), 8.08 (s, 1H).

Intermediate Ex. 31: 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetic acid (FIG. 1AP)

TABLE 1.14 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 31a methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetate Step 1: methyl 2-(3-amino-4-hydroxyphenyl)acetate (300 mg, 1.66 mmol) was suspended in water (4 mL). Dinibyl sulfone (200 μL, 1.99 mmol), boric acid (62 mg, 1.00 mmol) and glycerol (109 μL, 1.49 mmol) were added and the mixture was heated to reflux for 20 h. The mixture was cooled to rt and the aqueous layer was extracted with EtOAc. The organic layer was concentrated to dryness and the crude was purified by column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness to afford methyl 2-[3-(1,1-dioxo-1- thiomorpholin-4-yl)-4-hydroxyphenyl]acetate Ex. 31a (482 mg, 96%) as an off white solid. Ex. 31 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetic acid Step 2: methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetate Ex. 31a (482 mg, 1.62 mmol) was dissolved in THF/H2O (4:1, 16 mL/4 mL). Lithium hydroxide monohydrate (136 mg, 3.25 mmol) was added and the mixture was stirred at rt for 16 h. THF was removed under vacuum. EtOAc and water were added followed by 1N HCl under vigorous stirring until pH 4 was reached. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude was purified by flash silica gel column chromatography eluting with a gradient of heptane/EtOAc from [100:0] to [0:100]. The product fractions were combined and concentrated to dryness to afford 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetic acid Ex. 31 (156 mg, 34%) as pale-brown solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.23-3.39 (m, 8H), 6.73-6.81 (m, 2H), 6.91 (s, 1H), 8.98 (s, 1H).

Intermediate Ex. 32: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methylpropanoic acid (FIG. 1AQ)

2-(4-Chlorophenyl)-2-methylpropanoic acid (500 mg, 2.52 mmol) was dissolved in dry toluene/tBuOH (5:1, 15 mL/3 mL). The mixture was purged with nitrogen. Thiomorpholine-1,1-dioxide (851 mg, 6.29 mmol), NaOtBu (845 mg, 8.81 mmol), Pd(OAc)2 (25 mg, 0.13 mmol) and XPhos (115 mg, 0.25 mmol) were added in a tube and this was closed under nitrogen atmosphere. The mixture was heated to 120° C. for 20 h. After cooling to rt, EtOAc and water were added followed by 1 N HCl under vigorous stirring until pH 4 was reached. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness to afford 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methylpropanoic acid Ex. 32 (510 mg, 68%) as white solid.

1H NMR (300 MHz, DMSO-d6, δ in ppm): 1.44 (s, 6H), 3.11 (br(s), 4H), 3.74 (br(s), 4H), 6.98 (d, 2H, J=8.7 Hz), 7.22 (d, 2H J=8.7 Hz).

Intermediate Ex. 33: 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclobutane-1-carboxylic acid (FIG. 1AR)

1-(4-chlorophenyl)cyclobutanecarboxylic acid (500 mg, 2.37 mmol) was dissolved in dry toluene/tBuOH (5:1, 15 mL/3 mL). The mixture was purged with nitrogen. Thiomorpholine-1,1-dioxide (802 mg, 5.93 mmol), NaOtBu (798 mg, 8.31 mmol), Pd(OAc)2 (27 mg, 0.12 mmol) and XPhos (113 mg, 0.24 mmol) were added in a tube and this was closed under nitrogen atmosphere. The mixture was heated to 120° C. for 20 h. After cooling to rt, EtOAc and water were added followed by 1 N HCl under vigorous stirring until pH 4 was reached. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness to afford 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclobutane-1-carboxylic acid Ex. 33 (619 mg, 84%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 1.69-1.96 (m, 2H), 2.26-2.40 (m, 2H), 2.60-2.73 (m, 2H), 3.11 (br(s), 4H), 3.75 (br(s), 4H), 6.99 (d, 2H, J=8.6 Hz), 7.16 (d, 2H, J=8.6 Hz).

Intermediate Ex. 36: 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetic acid (FIG. 1AS)

TABLE 1.15 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 36a 4-(6-bromopyridin-3-yl)-1-thiomorpholine-1,1-dione Step 1: 2-bromo-5-iodopyridine (1.24 g, 4.35 mmol), thiomorpholine-1,1-dioxide (882 mg, 6.53 mmol) and NaOtBu (1.04 g, 10.87 mmol) were charged to a screw cap tube, dry toluene (25 mL) was added and the mixture was degassed by nitrogen bubbling for 5 min. Then XantPhos (250 mg, 0.44 mmol) and Pd2(dba)3 (200 mg, 0.22 mmol) were incorporated and the tube was closed under nitrogen atmosphere. The reaction mixture was stirred at rt for 4 days. EtOAc and water were added. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was absorbed on silica gel and purified by column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [95:5]. The product fractions were combined and concentrated to dryness to afford 4-(6-bromopyridin-3-yl)-1-thiomorpholine-1,1-dione Ex. 36a (730 mg, 57%) as yellow solid. Ex. 36b methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetate Step 2: 4-(6-bromopyridin-3-yl)-1-thiomorpholine-1,1-dione Ex. 36a (630 mg, 2.16 mmol), methyl acetoacetate (694 μL, 6.49 mmol) and K3PO4 (1.83 g, 8.65 mmol) were charged to a screw cap tube, dry toluene (20 mL) was added and the mixture was degassed by nitrogen bubbling for 5 min. Then Pd(OAc)2 (25 mg, 0.11 mmol) and di-tert-butyl XPhos (98 mg, 0.22 mmol) were incorporated and the tube was closed under nitrogen atmosphere. The reaction mixture was stirred at 120° C. for 20 h. The reaction was quenched with EtOAc/H2O. After phase separation, the combined organic layers were washed with brine, dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [90:10]. The desired fractions were combined and concentrate to afford methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetate Ex. 36b (445 mg, 72%) as brown oil. Ex. 36 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetic acid Step 3: methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]acetate Ex. 36b (445 mg, 1.56 mmol) was dissolved in THF/H2O (4:1, 8 mL/4 mL). Lithium hydroxide monohydrate (131 mg, 3.13 mmol) was added and the mixture was stirred at rt for 16 h. The crude was absorbed directly onto silica gel and purified by silica gel column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/MeOH from [100:0] to [75:25]. The product fractions were combined and concentrated to dryness. The resultant product was triturated in Et2O and dried under vacuum at constant weight to give 2-[5-(1,1-dioxo-1-thiomorpholin- 4-yl)pyridin-2-yl]acetic acid Ex. 36 (149 mg, 35%) as yellow solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 3.14 (m, 4H), 3.53 (br(s), 2H), 3.77 (br(s), 4H), 7.17-7.20 (m, 1H), 7.38-7.41 (m, 1H), 8.23 (s, 1H).

Intermediate Ex. 37: 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid (FIG. 1AT)

TABLE 1.16 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 37a bromo[1-(methoxycarbonyl)cyclopropyl]zinc Step 1: to a solution of Zn dust (3.0 g, 30.26 mmol) in dry THF (25 mL) at rt was added 1,2-dibromoethane (434 μL, 5.04 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 70° C. for 1 min and cooled down to rt. This procedure was repeated 5 times. Me3SiCl (256 μL, 2.02 mmol) was added and the resulting suspension was stirred at rt for 15 min. It was the heated to 65° C. and a few drops of methyl 1-bromocyclopropanecarboxylate were added. A solution of methyl 1-bromocyclopropanecarboxylate (2.61 mL, 25.22 mmol) in dry THF (5 mL) was added at such a rate that reflux was maintained. Upon completion of addition, the reaction mixture was refluxed for an additional 20 min and allowed to cool down to rt. The zinc was allowed to settle and the supernatant was used as such. Complete conversion was assumed. Ex. 37b 4-(5-bromopyrimidin-2-yl)-1-thiomorpholine-1,1-dione Step 2: DIPEA (675 μL, 3.88 mmol) was added to 5-bromo-2-chloropyrimidine (500 mg, 2.58 mmol) in CH3CN (10 mL). Then, thiomorpholine-1,1-dioxide (349 mg, 2.58 mmol) was added to the mixture. The solution was heated at 50° C. for 72 h. The solvent was removed and H2O followed by EtOAc were added to the crude. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by silica gel column chromatography eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness to afford 4-(5-bromopyrimidin-2-yl)-1- thiomorpholine-1,1-dione Ex. 37b (388 mg, 51%) as white solid. Ex. 37c methyl 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1- carboxylate Step 3: 4-(5-bromopyrimidin-2-yl)-1-thiomorpholine-1,1-dione Ex. 37b (388 mg, 1.33 mmol), bromo[1-(methoxycarbonyl)cyclopropyl]zinc Ex. 37a (5 mL, 3.98 mmol) and dry THF (5 mL) were placed in flask, the mixture was degassed by nitrogen bubbling for 5 min. Then XPhos (127 mg, 0.27 mmol) and Pd2(dba)3 (122 mg, 0.13 mmol) were incorporated and the reaction mixture was stirred at 75° C. for 16 h. The reaction mixture was concentrated and the residue was diluted with EtOAc/H2O. The phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash chromatography on silica eluting with heptane and a gradient of heptane/EtOAc from [100:0] to [50:50]. The desired fractions were combined and concentrate to obtain methyl 1-[2-(1,1-dioxo-1- thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylate Ex. 37c (312 mg, 76%) as white solid. Ex. 37 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Step 4: Lithium hydroxide monohydrate (126 mg, 3.01 mmol) was added to the mixture of methyl 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5- yl]cyclopropane-1-carboxylate Ex. 37c (312 mg, 1.00 mmol) in THF/H2O (2:1, 10 mL/5 mL) at 0° C. Then, the mixture was stirred at rt for 18 h. EtOAc and water was added to the mixture. Then, 1N HCl was added to the solution under vigorous stirring until pH 2 was reached. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness. The aqueous layer was concentrated to dryness. Two solids collected were purified by silica gel column chromatography eluting with CH2Cl2 and a gradient of CH2Cl2/methanol [100:0] to [90:10] yielding 1-[2-(1,1-dioxo-1-thiomorpholin-4- yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Ex. 37 (164 mg, 55%) as white solid. 1H NMR (300 MHz, DMSO-d6, δ in ppm): 1.15 (m, 2H), 1.45 (m, 2H), 3.14 (m, 4H), 4.21 (m, 4H), 8.39 (s, 2H), 12.50 (s, 1H).

Intermediate Ex. 41: 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid (FIG. 1AU)

TABLE 1.17 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 41a 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Step 1: methyl 1-(3-bromophenyl)cyclopropane-1-carboxylate was dissolved in dry toluene (15 mL) and the mixture was purged with N2. Thiomorpholine-1,1- dioxide (757 mg, 5.60 mmol), sodium tert-butoxide (538 mg, 5.60 mmol), Pd(OAc)2 (42 mg, 0.19 mmol) and XantPhos (216 mg, 0.37 mmol) were added and the solution was degassed by bubbling N2 for 5 min. The solution was heated at 110° C. for 16 h. After the completion of the reaction, the solution was cooled to rt and quenched with EtOAc and water. The combined organic layer was concentrated to dryness. No purification could be done as no separation was observed. The compound obtained as crude was 1-[3-(1,1-dioxo-1- thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 41a (1.05 g). Ex. 41b methyl 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1- carboxylate Step 2: the crude 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1- carboxylic acid Ex. 41a (1.05 g) was dissolved in MeOH (25 mL). HCl (4M in dioxane) (5 mL) was added and the mixture was heated overnight at 50° C. The mixture was concentrated to dryness. The crude material was partitioned between EtOAc and sat. NaHCO3 solution. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The resulting oil was purified by column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [80:20]. The product fractions were combined and concentrated to dryness to afford methyl 1-[3-(1,1-dioxo-1-thiomorpholin-4- yl)phenyl]cyclopropane-1-carboxylate Ex. 41b (333 mg, 21% over two steps) as brown solid. Ex. 41 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Step 3: lithium hydroxide monohydrate (135 mg, 3.23 mmol) was added to the mixture of methyl 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1- carboxylate Ex. 41b (333 mg, 1.08 mmol) in THF/H2O (2:1, 10 mL/5 mL) at 0° C. Then, the mixture was stirred at rt for 18 h. The mixture was concentrated to dryness. Then, water and 1N HCl was added to the solution under vigorous stirring until pH = 2 was reached. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness. The aqueous layer was concentrated to dryness. Two solids collected were purified by silica gel column chromatography eluting with a gradient of CH2Cl2/methanol [100:0] to [90:10] yielding 1-[3-(1,1-dioxo-1- thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid Ex. 41 (219 mg, 69%) as white solid. 1H NMR (300 MHz, DMSO-d6, d ppm): 1.13 (m, 2H), 1.40 (m, 2H), 3.11 (s, 4H), 3.75 (s, 4H), 6.79 (m, 1H), 6.89 (m, 1H), 6.96 (s, 1H), 7.16 (m, 1H), 12.22 (br(s), 1H).

Intermediate Ex. 43: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]acetic acid

(FIG. 1AV)

TABLE 1.18 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 43a ethyl 2-(bromozincio)acetate Step 1: to a solution of zinc dust (4.0 g, 40.35 mmol) in dry THF (30 mL) was added at rt 1,2-dibromoethane (579 μL, 6.72 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 70° C. for 1 min and cooled down to rt. This procedure was repeated 5 times. Me3SiCl (341 μL, 2.69 mmol) was added and the resulting suspension was stirred at rt for 15 min. It was then heated to 65° C. and a few drops of ethyl 2-bromoacetate were added. Then a solution of ethyl 2- bromoacetate (3.73 mL, 33.62 mmol) in dry THF (10 mL) was added at such a rate that reflux was maintained. Upon completion of addition, the reaction mixture was refluxed for an additional 20 min and allowed to cool down to rt. The zinc was allowed to settle and the supernatant was used further without any analysis. Complete conversion was assumed. Ex. 43b 1-((5-bromo-2-nitrophenoxy)methyl)benzene Step 2: a solution of 5-bromo-2-nitrophenol (3.00 g, 13.76 mmol), benzyl bromide (1.96 mL, 16.51 mmol) and K2CO3 (2.85 g, 20.64 mmol) were taken up in acetone (20 mL) and heated at reflux for 5 h. After cooling to rt, the reaction mixture was concentrated to dryness. Then, the mixture was diluted with water and the aqueous solution was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [20:80]. The combined fractions were concentrated to dryness to afford 1-((5-bromo-2-nitrophenoxy)methyl)benzene Ex. 43b (2.99 g, 71%) as yellow solid. Ex. 43c 2-(benzyloxy)-4-bromobenzenamine Step 3: 1-((5-bromo-2-nitrophenoxy)methyl)benzene Ex. 43b (1.00 g, 3.25 mmol) was dissolved in EtOH (10 mL) and H2O (3 mL). Then, ammonium chloride (174 mg, 3.25 mmol) was added. The mixture was stirred at 35° C. for 20 min. After, iron (453 mg, 8.11 mmol) was added and the mixture was stirred at 50° C. for l h. Then, the reaction mixture was stirred at rt 16 h. The crude was filtered through a plug of Celite. Then, the mixture was partitioned between water and EtOAc. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [50:50]. The product fractions were combined and concentrated to dryness to afford 2- (benzyloxy)-4-bromobenzenamine Ex. 43c (833 mg, 92%) as brown oil. Ex. 43d 4-[2-(benzyloxy)-4-bromophenyl]-1-thiomorpholine-1,1-dione Step 4: afford 2-(benzyloxy)-4-bromobenzenamine Ex. 43c (833 mg, 2.99 mmol) was suspended in water (30 mL). Divinylsulfone (361 μL, 3.59 mmol), boric acid (111 mg, 1.80 mmol) and glycerol (248 mg, 2.70 mmol) were added and the reaction mixture was heated at reflux for 20 h. After TLC, some starting material was remaining. More divinylsulfone (361 μL, 3.59 mmol) was added and the mixture was heated to reflux for additional two days. LCMS showed full consumption of the starting material. The mixture was cooled to rt. EtOAc and water was added to the mixture. The organic layer was separated, washed with brine, dried over MgSO4, filtered and the solution was concentrated to dryness. Then, the crude material was purified by column chromatography on silica gel eluting with Heptane/EtOAc from [100:0] to [40:60]. The product fractions were concentrated under reduced pressure to afford 4-[2-(benzyloxy)-4- bromophenyl]-1-thiomorpholine-1,1-dione Ex. 43d (1.04 g, 87%) as brown solid. Ex. 43e ethyl 2-[3-(benzyloxy)-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetate Step 5: 4-[2-(benzyloxy)-4-bromophenyl]-1-thiomorpholine-1,1-dione Ex. 43d (500 mg, 1.26 mmol), ethyl 2-(bromozincio)acetate Ex. 43a (4.5 mL, 3.79 mmol) and dry THF (5 mL) were placed in flask, the mixture was degassed by N2 bubbling for 5 min. Then Pd2(dba)3 (115 mg, 0.13 mmol) and XPhos (120 mg, 0.25 mmol) were incorporated and the reaction mixture was stirred at 75° C. for 16 h. The reaction mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O. The two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [0:100]. The desired fractions were combined and concentrated to obtain ethyl 2-[3-(benzyloxy)-4-(1,1-dioxo- 1-thiomorpholin-4-yl)phenyl]acetate Ex. 43e (117 mg, 23%) as yellow oil. Ex. 43f ethyl 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]acetate Step 6: ethyl 2-[3-(benzyloxy)-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetate Ex. 43e (117 mg, 0.29 mmol) and Pd/C (30% w/w) were mixed in MeOH (3 mL) and the mixture was stirred at rt for 20 h under H2 atmosphere. The mixture was filtered through a plug of Celite. The crude material was purified by flash chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [0:100]. The product fractions were combined and concentrated to dryness to afford ethyl 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3- hydroxyphenyl]acetate Ex. 43f (54 mg, 59%) as brown oil. Ex. 43 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]acetic acid Step 7: lithium hydroxide monohydrate (22 mg, 0.52 mmol) was added to the mixture of ethyl 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]acetate Ex. 43f (54 mg, 0.17 mmol) in THF/H2O (2:1, 5 mL/2.5 mL) at 0° C. Then, the mixture was stirred at rt for 18 h. The mixture was concentrated to dryness. Then, water and 1N HCI was added to the solution under vigorous stirring until pH = 2 was reached. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness yielding 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3- hydroxyphenyl]acetic acid Ex. 43 (37 mg, 75% (crude)) as brown solid. 1H NMR (300 MHz, DMSO-d6, d in ppm): 3.27 (s, 4H), 3.41 (s, 2H), 6.64 (m, 1H), 6.74 (s, 1H), 6.95 (m, 1H), 9.01 (s, 1H).

Intermediate Ex. 44: 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]acetic acid (FIG. 1AW)

TABLE 1.19 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex. 44a (2-amino-4-bromophenyl)methanol Step 1: a solution of methyl 2-amino-4-bromobenzoate (500 mg, 2.17 mmol) in dry THF (10 mL) was cooled at −10° C. Then, a solution of lithium aluminium hydride (1M in THF) (6.5 mL, 6.52 mmol) was added dropwise to the solution. The mixture was allowed to reach rt and the solution was stirred at rt overnight. The reaction was cooled down with a ice water bath and quenched with a mixture of MeOH and sat. solution of sodium potassium tartrate. The solution was stirred at rt for additional 6 h. The reaction mixture was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness to afford (2- amino-4-bromophenyl)methanol Ex. 44a (326 mg, 74%) as sticky brown solid. Ex. 44b 4-[5-bromo-2-(hydroxymethyl)phenyl]-1-thiomorpholine-1,1-dione Step 2: (2-amino-4-bromophenyl)methanol Ex. 44a (326 mg, 1.61 mmol) was suspended in water (4 mL). Divinylsulfone (325 μL, 3.22 mmol), boric acid (60 mg, 0.97 mmol) and glycerol (133 mg, 1.45 mmol) were added and the reaction mixture was heated at reflux for 20 h. The mixture was cooled to rt. EtOAc and water was added to the mixture. The organic layer was separated, washed with brine, dried over MgSO4, filtered and the solution was concentrated to dryness. Then, the crude material was purified by flash column chromatography on silica gel eluting with Heptane/EtOAc from [100:0] to [0:100]. The desired fractions were concentrated under reduced pressure to afford 4-[5-bromo-2- (hydroxymethyl)phenyl]-1-thiomorpholine-1,1-dione Ex. 44b (290 mg, 56%). Ex. 44c 4-[5-bromo-2-(methoxymethyl)phenyl]-1-thiomorpholine-1,1-dione Step 3: 4-[5-bromo-2-(hydroxymethyl)phenyl]-1-thiomorpholine-1,1-dione Ex. 44b (290 mg, 0.91 mmol) was dissolved in dry DMF (4 mL) and the solution was cooled to 0-5° C. Sodium hydride (60% in mineral oill) was added under N2 atmosphere. After 15 min, when the gas evolution had ceased, a solution of iodomethane (62 μL, 1.00 mmol) was added and the mixture was allowed to warm to rt. The reaction mixture was stirred for additional 3 h. The reaction was quenched with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [60:40]. The desired fractions were combined and concentrated to obtain 4-[5-bromo-2- (methoxymethyl)phenyl]-1-thiomorpholine-1,1-dione Ex. 44c (197 mg, 65%) as sticky white solid. Ex. 44d methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]acetate Step 4: 4-[5-bromo-2-(methoxymethyl)phenyl]-1-thiomorpholine-1,1-dione Ex. 44c (150 mg, 0.46 mmol), methyl acetoacetate (147 μL, 1.37 mmol) and potassium phosphate (390 mg, 1.83 mmol) were charged to a screw cap tube, dry toluene (6 mL) was added and the mixture was degassed by N2 bubbling for 5 min. Then Pd(OAc)2 (6 mg, 0.02 mmol) and di-tert-butyl XPhos (21 mg, 0.05 mmol) were incorporated and the tube was closed under N2 atmosphere. The reaction mixture was stirred at 120° C. for 16 h. The mixture was joined to a previous experiment. EtOAc/H2O were added to the solution. The two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [40:60]. The desired fractions were combined and concentrated to obtain methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (methoxymethyl)phenyl]acetate Ex. 44d (105 mg, 55%, calculated over 197 mg of starting material) as yellow oil. Ex. 44 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]acetic acid Step 5: lithium hydroxide monohydrate (13 mg, 0.32 mmol) was added to the mixture of methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (methoxymethyl)phenyl]acetate Ex. 44d (105 mg, 0.32 mmol) in THF/H2O (3:1, 3 mL/1 mL) at 0° C. Then, the mixture was stirred at rt for 18 h. The mixture was concentrated to dryness. Then, water and 1N HCl was added to the solution under vigorous stirring until pH = 4 was reached. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness yielding 2-[3-(1,1-dioxo-1- thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]acetic acid Ex. 44 (95 mg, 94%) as yellow oil. 1H NMR (300 MHz, DMSO-d6, d in ppm): 3.13 (br(s), 4H), 3.34 (s, 3H), 3.42 (br(s), 4H), 3.56 (s, 2H), 4.40 (s, 2H), 6.99 (s, 1H), 7.02 (d, 1H, J = 7.7 Hz), 7.31 (d, 1H, J = 7.7 Hz).

Intermediate Ex. 45: 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]acetic acid (FIG. 1AX)

TABLE 1.20 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.45a 4-(5-bromo-2-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-1-thiomorpholine- 1,1-dione Step 1: imidazole (230 mg, 3.43 mmol) was added to a solution of 4-[5-bromo-2- (hydroxymethyl)phenyl]-1-thiomorpholine-1,1-dione (500 mg, 1.56 mmol) suspended in DMF (20 mL). The solution was cooled to 0° C. Tert-butyl dimethyl silyl chloride (350 mg, 2.34 mmol) diluted in small amount of DMF was added dropwise to the solution. The reaction mixture was stirred at rt for 16 h. The reaction was quenched with EtOAC/H20. After phase separation, the combined organic layers were washed with brine, dried over MgSO4, filtered and were concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [80:20]. The desired fractions were combined and concentrated to afford 4-(5-bromo-2-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-1- thiomorpholine-1,1-dione Ex.45a (417 mg, 62%) as white solid. Ex.45b methyl 2-(4-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(1,1-dioxo-1- thiomorpholin-4-yl)phenyl)acetate Step 2: 4-(5-bromo-2-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-1- thiomorpholine-1,1-dione Ex.45a (417 mg, 0.96 mmol), methyl acetoacetate (310 μL, 2.88 mmol) and potassium phosphate (815 mg, 3.84 mmol) were charged to a screw cap tube, dry toluene (10 mL) was added and the mixture was degassed by N2 bubbling for 5 min. Then Pd(OAc)2 (11 mg, 0.05 mmol) and di-tert-butyl XPhos (41 mg, 0.10 mmol) were incorporated and the tube was closed under N2 atmosphere. The reaction mixture was stirred at 120° C. for 16 h. The mixture was joined to a previous experiment. EtOAc/H2O were added to the solution. The two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [80:20]. The desired fractions were combined and concentrated to obtain methyl 2-(4-{[(tert- butyldimethylsilyl)oxy]methyl}-3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl)acetate Ex.45b (290 mg, 71%) as yellow oil. Ex.45c methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (hydroxymethyl)phenyl]acetate Step 3: tetrabutylammonium fluoride solution (1.0M in THF) (1.36 mL, 1.36 mmol) was added to methyl 2-(4-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(1,1- dioxo-1-thiomorpholin-4-yl)phenyl)acetate Ex.45b (290 mg, 0.68 mmol) diluted in THF (5 mL). The reaction mixture was stirred at rt for 70 h. The solution was concentrated to dryness and the residue was diluted with EtOAc/H2O. The two phases were separated. The organic layer was washed with brine several times. The organic phase was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [0:100]. The desired fractions were combined and concentrated under reduced pressure to obtain methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (hydroxymethyl)phenyl]acetate Ex.45c (95 mg, 45%) as colorless oil. Ex.45 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]acetic acid Step 4: lithium hydroxide monohydrate (25 mg, 0.61 mmol) was added to the mixture of methyl 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (hydroxymethyl)phenyl]acetate Ex.45c (95 mg, 0.30 mmol) in THF/H2O (3:1, 3 mL/1 mL) at 0° C. Then, the mixture was stirred at rt for 18 h. The mixture was concentrated to dryness. Then, water and 1N HCl was added to the solution under vigorous stirring until pH = 4 was reached. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness yielding 2-[3-(1,1-dioxo-1- thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]acetic acid Ex.45 (62 mg, 68%) as white solid. 1H NMR (300 MHz, DMSO-d6, d in ppm): 3.28 (m, 8H), 3.53 (s, 2H), 4.55 (s, 2H), 5.06 (br(s), 1H), 7.01 (d, 1H, J = 7.8 Hz), 7.05 (s, 1H), 7.37 (d, 1H, J = 7.8 Hz).

Intermediate Ex. 46: 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetic acid (FIG. 1AY)

TABLE 1.21 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.46a 1-tert-butyl 3-methyl 2-(5-bromopyrimidin-2-yl)malonate Step 1: sodium hydride (60% in mineral oil) (310 mg, 7.76 mmol) was added portionwise to a stirred solution of tert-butyl methyl malonate (1.05 mL, 6.20 mmol) in dry DMF (25 mL) at 0° C. and under N2 atmosphere. The solution was stirred at rt for 15 min and 2-chloro-5-bromopyrimidine (1.0 g, 5.17 mmol) was added portionwise. The reaction mixture was stirred at 50° C. for 3 h. After cooling to rt, sat. NH4Cl and water was added to quench the reaction. The solution was acidified up to pH = 3 by the addition of 2N HCl. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and the solution was concentrated to dryness affording 1-tert-butyl 3-methyl 2-(5-bromopyrimidin-2-yl)malonate Ex.46a. The crude material was considered to be suitable for the next synthetic step. Ex.46b methyl 2-(5-bromopyrimidin-2-yl)acetate Step 2: 1-tert-butyl 3-methyl 2-(5-bromopyrimidin-2-yl)malonate Ex.46a (1.88 g, crude) was dissolved in CH2Cl2 (20 mL). The mixture was cooled to 0° C. and trifluoroacetic acid 99% (10 mL) was added dropwise. The reaction mixture was allowed to rise rt and stirred at this temperature for 4 h. The solvent was removed under reduced pressure. Toluene was added and the solution was evaporated to dryness. The residue was diluted with EtOAc and sat. sodium bicarbonate solution. The two phases were partitionated. The organic layer was washed with brine, dried over MgSO4 and the solution was concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of Heptane/EtOAc from [100:0] to [60:40]. The desired fractions were combined and concentrated to obtain methyl 2-(5-bromopyrimidin-2-yl)acetate Ex.46b (405 mg, 34%, calculated over two steps) as yellow oil. Ex.46c methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetate Step 3: methyl 2-(5-bromopyrimidin-2-yl)acetate Ex.46b (355 mg, 1.53 mmol), thiomorpholine-1,1-dioxide (310 mg, 2.30 mmol) and Cs2CO3 (1.0 g, 3.06 mmol) were charged to a screw cap tube, dry toluene (10 mL) was added and the mixture was degassed by N2 bubbling for 5 min. Then Pd2(dba)3 (70 mg, 0.08 mmol) and XPhos (73 mg, 0.15 mmol) were incorporated and the tube was closed under N2 atmosphere. The reaction mixture was stirred at 120° C. for 16 h. The solution was diluted with EtOAc and washed with water and brine. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel using as eluent Heptane/EtOAc. The desired fractions were collected and concentrated to dryness affording methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4- yl)pyrimidin-2-yl]acetate Ex.46c (105 mg, 24%) as orange solid. Ex.46 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetic acid Step 4: lithium hydroxide monohydrate (32 mg, 0.74 mmol) was added to the mixture of methyl 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetate Ex.46c (105 mg, 0.37 mmol) in THF/H2O (5 mL/3 mL) at 0° C. Then, the mixture was stirred overnight at rt. The mixture was concentrated to dryness. Then, water and 1N HCl was added to the solution under vigorous stirring until pH = 4 was reached. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried over MgSO4, filtered and the solution was concentrated to dryness. The aqueous layer was concentrated under reduced pressure. The obtained solid was triturated with tert-butyl methyl ester and then filtered off to afford 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]acetic acid Ex.46 (81 mg, 81%) as white solid. 1H NMR (300 MHz, DMSO-d6, d in ppm): 3.12 (s, 4H), 3.64 (s, 2H), 3.85 (s, 4H), 8.52 (m, 2H).

Intermediate Ex. 49: 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1-carboxylic acid (FIG. 1AZ)

TABLE 1.22 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.49a 4-(5-bromo-2-methoxyphenyl)-1-thiomorpholine-1,1-dione Step 1: water (5 mL), boric acid (55 mg, 0.89 mmol) and glycerol (2-3 drops) were added to a stirred solution of 5-bromo-2-methoxyaniline (600 mg, 2.97 mmol) and divinylsulfone (351 mg, 2.97 mmol). The resulting mixture was stirred at reflux for 18 h. The reaction mixture was cooled to rt and extracted with EtOAc. The organic layer was washed three times with water, dried over MgSO4, filtered and the solution was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography using Hexanes/EtOAc (50:50) as eluent yielding 4-(5-bromo-2-methoxyphenyl)-1- thiomorpholine-1,1-dione Ex.49a (900 mg, 95%). 1H NMR (400 MHz, DMSO- d6, d in ppm): 3.22 (t, 4H, J = 5.2 Hz), 3.41-3.46 (m, 4H), 3.80 (s, 3H), 6.92-6.96 (m, 1H), 7.12 (d, 1H, J = 2.4 Hz), 7.18 (dd, 1H, J = 8.6 Hz, J = 2.4 Hz). Ex.49b methyl 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- methoxyphenyl]cyclopropane-1-carboxylate Step 2: 4-(5-bromo-2-methoxyphenyl)-1-thiomorpholine-1,1-dione Ex.49a (900 mg, 2.81 mmol), Pd2(dba)3 (257 mg, 0.28 mmol), Xphos (268 mg, 0.56 mmol) were charged to a screw cap tube and dry THF (15 mL) was added and the mixture was degassed by N2 bubbling for 5 min. To this solution freshly prepared bromo[1-(methoxycarbonyl)cyclopropyl]zinc (2.06 g, 8.43 mmol) was added dropwise. The reaction mixture was stirred at 75° C. for 16 h. After cooling to rt, the mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30] to [50:50]. The desired fractions were combined and concentrated to obtain methyl 1-[3-(1,1-dioxo-1- thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1-carboxylate Ex.49b (710 mg, 74%) as yellow solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.17 (m, 2H), 1.43 (q, 2H, J = 3.9 Hz), 3.21 (t, 4H, J = 5.2 Hz), 3.41 (dd, 4H, J = 7.1 Hz, J = 3.4 Hz), 3.54 (s, 3H), 3.80 (s, 3H), 6.89 (d, 1H, J = 8.3 Hz), 6.93 (d, 1H, J = 2.1 Hz), 6.97 (dd, 1H, J = 8.3 Hz, J = 2.1 Hz). Ex.49 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1- carboxylic acid Step 3: lithium hydroxide monohydrate (263 mg, 6.28 mmol) was added to the mixture of methyl 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- methoxyphenyl]cyclopropane-1-carboxylate Ex.49b (710 g, 2.09 mmol) in THF (50 mL) and H2O (25 mL) at 0° C. Then, the mixture was stirred at rt overnight. EtOAc and water was added to the mixture. Then, 3M HCl was added to the mixture under vigorous stirring until pH = 2 was reached. The organic layer was separated, and the aqueous layer was extracted with EtOAc, and next with 50% MeOH in CH2Cl2 (3 times). The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30], [50:50] to [0:100]. The desired fractions were combined and concentrated to obtain 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)- 4-methoxyphenyl]cyclopropane-1-carboxylic acid Ex.49 (532 mg, 78%) as pale brown solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.09 (q, 2H, J = 3.7 Hz), 1.39 (q, 2H, J = 3.8 Hz), 3.21 (t, 4H, J = 5.1 Hz), 3.41 (dd, 4H, J = 7.0 Hz, J = 3.4 Hz), 3.79 (s, 3H), 6.88 (d, 1H, J = 8.3 Hz), 6.92 (d, 1H, J = 2.1 Hz), 6.96 (dd, 1H, J = 8.2 Hz, J = 2.1 Hz), 12.20 (s, 1H).

Intermediate Ex. 50: 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1-carboxylic acid (FIG. 1BA)

TABLE 1.23 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.50a 4-(3-bromo-4-methylphenyl)-1-thiomorpholine-1,1-dione Step 1: water (8.5 mL), boric acid (100 mg, 1.61 mmol) and glycerol (2-3 drops) were added to a stirred solution of 3-bromo-4-methylaniline (1.00 g, 5.37 mmol) and divinylsulfone (635 mg, 5.37 mmol). The resulting mixture was stirred at reflux for 18 h. The reaction mixture was cooled to rt and extracted with EtOAc. The organic layer was washed three times with water, dried over MgSO4, filtered and the solution was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography using Hexanes/EtOAc (50:50) as eluent yielding 4-(3-bromo-4-methylphenyl)-1-thiomorpholine-1,1- dione Ex.50a (1.45 g, 89%). 1H NMR (400 MHz, DMSO-d6, d in ppm): 2.25 (s, 3H), 3.07-3.14 (m, 4H), 3.72-3.78 (m, 4H), 6.93-6.99 (m, 1H), 7.20 (d, 1H, J = 8.6 Hz), 7.23 (d, 1H, J = 2.7 Hz). Ex.50b methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane- 1-carboxylate Step 2: 4-(3-bromo-4-methylphenyl)-1-thiomorpholine-1,1-dione Ex.50a (1.45 g, 4.77 mmol), Pd2(dba)3 (436 mg, 0.48 mmol), Xphos (454 mg, 0.95 mmol) were charged to a screw cap tube and dry THF (15 mL) was added and the mixture was degassed by N2 bubbling for 5 min. To this solution freshly prepared bromo[1-(methoxycarbonyl)cyclopropyl]zinc (3.50 g, 14.30 mmol) was added dropwise. The reaction mixture was stirred at 75° C. for 16 h. After cooling to rt, the mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30] to [50:50]. The desired fractions were combined and concentrated to obtain methyl 1-[5-(1,1-dioxo-1- thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1-carboxylate Ex.50b (1.35 g, 88%) as pale brown solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.20 (dd, 2H, J = 4.0 Hz, J = 2.8 Hz), 1.52 (d, 2H, J = 3.3 Hz), 2.15 (s, 3H), 3.11 (dd, 4H, J = 6.7 Hz, J = 3.8 Hz), 3.54 (s, 3H), 3.67-3.73 (m, 4H), 6.83 (dd, 1H, J = 8.2 Hz, J = 2.7 Hz), 6.89 (d, 1H, J = 2.7 Hz), 7.04 (d, 1H, J = 8.3 Hz). Ex.50 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1- carboxylic acid Step 3: lithium hydroxide monohydrate (525 mg, 12.52 mmol) was added to the mixture of methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- methylphenyl]cyclopropane-1-carboxylate Ex.50b (1.35 g, 4.17 mmol) in THF (50 mL) and H2O (25 mL) at 0° C. Then, the mixture was stirred at rt overnight. EtOAc and water was added to the mixture. Then, 3M HCl was added to the mixture under vigorous stirring until pH = 2 was reached. The organic layer was separated, and the aqueous layer was extracted with EtOAc, and next with 50% MeOH in CH2Cl2 (3 times). The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30], [50:50] to [0:100]. The desired fractions were combined and concentrated to obtain 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)- 2-methylphenyl]cyclopropane-1-carboxylic acid Ex.50 (490 mg, 38%) as yellow solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.12 (s, 2H), 1.47 (d, 2H, J = 3.6 Hz), 2.18 (s, 3H), 3.08-3.14 (m, 4H), 3.66-3.73 (m, 4H), 6.82 (dd, 1H, J = 8.2 Hz, J = 2.7 Hz), 6.87 (d, 1H, J = 2.7 Hz), 7.03 (d, 1H, J = 8.3 Hz), 12.22 (s, 1H).

Intermediate Ex. 51: 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1-carboxylic acid (FIG. 1BB)

TABLE 1.24 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.51a 4-(6-chloro-2-methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Step 1: water (25 mL), boric acid (434 mg, 7.01 mmol) and glycerol (10-15 drops) were added to a stirred solution of 6-chloro-2-methylpyridin-3-amine (2.00 g, 14.03 mmol) and divinylsulfone (1.66 g, 14.03 mmol). The resulting mixture was stirred at reflux for 18 h. The reaction mixture was cooled to rt and extracted with EtOAc. The organic layer was washed three times with water, dried over MgSO4, filtered and the solution was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [4:1] to [3:1] yielding 4-(6-chloro- 2-methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.51a (2.10 g, 57%) as pale brown solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 2.46 (s, 3H), 3.30-3.32 (m, 8H), 7.28 (dd, 1H, J = 8.4 Hz, J = 0.8 Hz), 7.61 (d, 1H, J = 8.4 Hz). Ex.51b methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2- yl]cyclopropane-1-carboxylate Step 2: 4-(6-chloro-2-methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.51a (1.30 g, 4.99 mmol), Pd2(dba)3 (457 mg, 0.50 mmol), Xphos (475 mg, 1.00 mmol) were charged to a screw cap tube and dry THF (15 mL) was added and the mixture was degassed by N2 bubbling for 5 min. To this solution freshly prepared bromo[1-(methoxycarbonyl)cyclopropyl]zinc (3.66 g, 14.96 mmol) was added dropwise. The reaction mixture was stirred at 75° C. for 16 h. After cooling to rt, the mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified on silica gel column chromatography eluting with a gradient of CH2Cl2/MeOH from [100:0], [99:1] to [98:2]. The desired fractions were combined and concentrated to obtain methyl 1-[5-(1,1- dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1-carboxylate Ex.51b (1.20 g, 74%) as pale brown solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.33 (q, 2H, J = 3.9 Hz), 1.46 (q, 2H, J = 3.9 Hz, J = 3.4 Hz), 2.44 (s, 3H), 3.30 (d, 8H, J = 3.0 Hz), 3.58 (s, 3H), 7.29 (dd, 1H, J = 8.2 Hz, J = 0.6 Hz), 7.48 (d, 1H, J = 8.2 Hz). Ex.51 1-[5-[1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1- carboxylic acid Step 3: lithium hydroxide monohydrate (466 mg, 11.10 mmol) was added to the mixture of methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2- yl]cyclopropane-1-carboxylate Ex.51b (1.20 g, 3.70 mmol) in THF (50 mL) and H2O (25 mL) at 0° C. Then, the mixture was stirred at rt overnight. EtOAc and water was added to the mixture. Then, 3M HCl was added to the mixture under vigorous stirring until pH = 2 was reached. The organic layer was separated, and the aqueous layer was extracted with EtOAc, and next with 50% MeOH in CH2Cl2 (3 times). The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30], [50:50] to [0:100]. The desired fractions were combined and concentrated to obtain 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2- yl]cyclopropane-1-carboxylic acid Ex.51 (533 mg, 46%) as pale brown solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.32 (q, 2H, J = 3.7 Hz), 1.48 (q, 2H, J = 3.7 Hz), 2.46 (s, 3H), 3.29-3.32 (m, 8H), 7.27 (d, 1H, J = 8.3 Hz), 7.52 (d, 1H, J = 8.4 Hz), 13.39 (s, 1H).

Intermediate Ex. 52: 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1-carboxylic acid (FIG. 1BC)

TABLE 1.25 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.52a 4-(6-chloro-5-methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Step 1: water (20 mL), boric acid (260 mg, 4.21 mmol) and glycerol (9-10 drops) were added to a stirred solution of 3-amino-6-chloro-4-picoline (2.00 g, 14.03 mmol) and divinylsulfone (1.66 g, 14.03 mmol). The resulting mixture was stirred at reflux for 18 h. The reaction mixture was cooled to rt and extracted with EtOAc. The organic layer was washed three times with water, dried over MgSO4, filtered and the solution was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography eluting with a gradient of Hexanes/EtOAc [80:20] to [40:60] yielding 4-(6-chloro-5- methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.52a (2.25 g, 62%) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 2.26 (s, 3H), 3.09- 3.16 (m, 4H), 3.78-3.85 (m, 4H), 7.49 (d, 1H, J = 2.4 Hz), 7.99 (d, 1H, J = 3.1 Hz). Ex.52b methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2- yl]cyclopropane-1-carboxylate Step 2: 4-(6-chloro-5-methylpyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.52a (200 mg, 0.77 mmol), Pd2(dba)3 (70 mg, 0.08 mmol), Xphos (73 mg, 0.15 mmol) were charged to a screw cap tube and dry THF (2.4 mL) was added and the mixture was degassed by N2 bubbling for 5 min. To this solution freshly prepared bromo[1-(methoxycarbonyl)cyclopropyl]zinc (562 mg, 2.3 mmol) was added dropwise. The reaction mixture was stirred at 75° C. for 16 h. After cooling to rt, the mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified on silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [50:50] to [20:80]. The desired fractions were combined and concentrated to obtain methyl 1-[5-(1,1-dioxo-1- thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1-carboxylate Ex.52b (940 mg, 50%) as yellowish oil. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.15- 1.20 (m, 2H), 1.48-1.50 (m, 2H), 2.21 (s, 3H), 3.10-3.16 (m, 4H), 3.55 (s, 3H), 3.76-3.82 (m, 4H), 7.28 (d, 1H, J = 2.2 Hz), 8.06 (d, 1H, J = 2.9 Hz). Ex.52 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1- carboxylic acid Step 3: lithium hydroxide monohydrate (365 mg, 8.70 mmol) was added to the mixture of methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2- yl]cyclopropane-1-carboxylate Ex.52b (940 mg, 2.90 mmol) in THF (28 mL) and H2O (14 mL) at 0° C. Then, the mixture was stirred 2 days at rt. EtOAc and water was added to the mixture. Then, 3M HCl was added to the mixture under vigorous stirring until pH = 2 was reached. The organic layer was separated, and the aqueous layer was extracted with EtOAc, and next with 50% MeOH in CH2Cl2 (3 times). The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of CH2Cl2/MeOH from [100:0] to [98:2]. The desired fractions were combined and concentrated to obtain 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2- yl]cyclopropane-1-carboxylic acid Ex.52 (210 mg, 23%) as white solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.20 (q, 2H, J = 3.8 Hz), 1.46 (q, 2H, J = 3.8 Hz), 2.25 (s, 3H), 3.11-3.16 (m, 4H), 3.74-3.81 (m, 4H), 7.26 (d, 1H, J = 2.8 Hz), 8.05 (d, 1H, J = 2.9 Hz), 12.27 (s, 1H).

Intermediate Ex. 53: 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxylic acid (FIG. 1BD)

TABLE 1.26 Starting compounds, Reaction conditions and purification, Cpd. Yield, Appearance, ¹H NMR (solvent) data Ex.53a 4-(6-chloropyridin-3-yl)-1-thiomorpholine-1,1-dione Step 1: water (30 mL), boric acid (866 mg, 14.00 mmol) and glycerol (12-15 drops) were added to a stirred solution of 5-amino-2-chloropyridine (3.00 g, 23.34 mmol) and divinylsulfone (2.34 mL, 23.34 mmol). The resulting mixture was stirred overnight at reflux. The reaction mixture was cooled to rt and extracted with EtOAc. The organic layer was washed three times with water, dried over MgSO4, filtered and the solution was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography eluting with a gradient of Hexanes/EtOAc from [70:30] to [50:50] yielding 4-(6- chloropyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.53a (3.60 g, 63%) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 3.10-3.17 (m, 4H), 3.80-3.85 (m, 4H), 7.32 (dd, 1H, J = 8.9 Hz, J = 0.5 Hz), 7.53 (dd, 1H, J = 8.9 Hz, J = 3.3 Hz), 8.17 (d, 1H, J = 3.2 Hz). Ex.53b methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1- carboxylate Step 2: 4-(6-chloropyridin-3-yl)-1-thiomorpholine-1,1-dione Ex.53a (2.50 g, 10.13 mmol), Pd2(dba)3 (928 mg, 1.01 mmol), Xphos (966 mg, 2.03 mmol) were charged to a screw cap tube and dry THF (30 mL) was added and the mixture was degassed by N2 bubbling for 5 min. To this solution freshly prepared bromo[1-(methoxycarbonyl)cyclopropyl]zinc (7.43 g, 30.40 mmol) was added dropwise. The reaction mixture was stirred at 75° C. for 16 h. After cooling to rt, the mixture was concentrated to dryness and the residue was diluted with EtOAc/H2O and the two phases were separated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified on silica gel column chromatography eluting with a gradient of CH2Cl2/MeOH from [100:0] to [98:2]. The desired fractions were combined and concentrated to obtain methyl 1-[5-(1,1-dioxo-1- thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxylate Ex.53b (600 mg, 19%) as orange oil. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.31 (q, 2H, J = 3.9 Hz), 1.45 (q, 2H, J = 3.8 Hz), 3.11-3.18 (m, 4H), 3.58 (s, 3H), 3.78-3.82 (m, 4H), 7.34-7.42 (m, 2H), 8.24 (dd, 1H, J = 2.9 Hz, J = 0.9 Hz). Ex.53 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxylic acid Step 3: lithium hydroxide monohydrate (243 mg, 5.80 mmol) was added to the mixture of methyl 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane- 1-carboxylate Ex.53b (600 mg, 1.93 mmol) in THF (18 mL) and H2O (9 mL) at 0° C. Then, the mixture was stirred overnight at rt. EtOAc and water was added to the mixture. Then, 3M HCl was added to the mixture under vigorous stirring until pH = 2 was reached. The organic layer was separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of CH2Cl2/MeOH from [100:0] to [98:2]. The desired fractions were combined and concentrated to obtain 1-[5-(1,1-dioxo-1-thiomorpholin-4- yl)pyridin-2-yl]cyclopropane-1-carboxylic acid Ex.53 (127 mg, 22%) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, d in ppm): 1.30 (q, 2H, J = 3.8 Hz), 1.46 (q, 2H, J = 3.7 Hz), 3.11-3.19 (m, 4H), 3.77-3.84 (m, 4H), 7.35 (d, 1H, J = 8.7 Hz), 7.43 (dd, 1H, J = 8.8 Hz, J = 3.1 Hz), 8.24 (d, 1H, J = 2.7 Hz), 13.16 (s, 1H).

Example 1b: Synthesis of Amine Intermediates for the Synthesis of Compounds According to the Invention

The following amines are commercially available The following amines were obtained following the procedure described in WO2006035157

TABLE 1.27 Ex.2 phenyl[2-(piperidin-1-yl)phenyl]methanamine The following amines were obtained following the procedure described in WO2016102633

TABLE 1.28 Ex.5 [4-methyl-2-(morpholin-4-yl)phenyl](phenyl)methanamine Ex.6 [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl) methanamine Ex.8 [4-methyl-2-(piperidin-1-yl)phenyl](phenyl)methanamine Ex.9 (2-bromo-4-methylphenyl)(phenyl)methanamine Ex.42 (5-methylfuran-2-yl)[2-(piperidin-1-yl)phenyl]methanamine Ex.54 3-methyl-1-[2-(piperidin-1-yl)phenyl]butan-1-amine

Intermediate Ex. 11: [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2A)

TABLE 1.29 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.11a 2-methyl-N-[(5-methylfuran-2-yl)methylidene]propane-2-sulfinamide Step 1: 5-methylfuran-2-carbaldehyde (1.0 g, 9.08 mmol) was dissolved in dry THF (5 mL). Titanium ethoxide (7.62 mL, 36.3 mmol) and 2-methyl-2-propane- sulfinamide (1.76 g, 14.5 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Brine was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure to afford 2-methyl-N-[(5-methylfuran- 2-yl)methylidene]propane-2-sulfinamide Ex.11a (1.70 g, 88%) as orange oil. The compound was used as such for the next step. Ex.11b 2-methyl-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2- yl)methyl}propane-2-sulfinamide Step 2: to a suspension of magnesium powder (120 mg, 4.94 mmol) in dry THF (small amount) was added dropwise 1-bromo-2-(trifluoromethyl)-4- methylbenzene (1.12 g, 4.69 mmol) diluted in dry THF (20 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, 2-methyl-N-[(5- methylfuran-2-yl)methylidene]propane-2-sulfinamide Ex.11a (500 mg, 2.34 mmol) diluted in THF (5 mL) was added to the solution. The reaction mixture was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of hexanes/EtOAc ([5:1] to [4:1]) to afford 2-methyl-N-{[4-methyl-2- (trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}propane-2-sulfinamide Ex.11b (533 mg, 61%). Ex.11 [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methanamine hydrochloride Step 3: to a solution of 2-methyl-N-{[4-methyl-2-(trifluoromethyl)phenyl](5- methylfuran-2-yl)methyl}propane-2-sulfinamide Ex.11b (533 mg, 1.43 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (0.9 mL) at 0° C. The reaction mixture was stirred at this temperature for 4 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2- yl)methanamine hydrochloride Ex.11 (322 mg, 55%) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 2.24 (d, 3H, J = 1.0 Hz), 2.43 (s, 3H), 5.59 (s, 1H), 6.10 (dd, 1H, J = 3.2 Hz, J = 1.2 Hz), 6.26 (d, 1H, J = 3.2 Hz), 7.67 (d, 2H, J = 6.9 Hz), 7.90 (d, 1H, J = 8.5 Hz), 9.25 (br(s), 3H). ″

Intermediate Ex. 12: (2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2A)

TABLE 1.30 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.12a N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2- sulfinamide Step 1: to a solution of 2-bromo-1-iodo-4-methylbenzene (1.74 g, 5.86 mmol) in dry THF (20 mL) was added a solution of isopropylmagnesium chloride 2M in THF (2.93 mL, 5.86 mmol) at −40° C. Then, 2-methyl-N-[(5-methylfuran-2- yl)methylidene]propane-2-sulfinamide Ex.11a (1.00 g, 4.69 mmol) diluted in dry THF (5 mL) was added dropwise at −40° C. The reaction was warmed to rt and stirred at that temperature for 3 days. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of hexanes/EtOAc ([8:2] to [6:4]) to afford N-[(2-bromo-4-methylphenyl)(5- methylfuran-2-yl)methyl]-2-methylpropane-2-sulfinamide Ex.12a (541 mg, 30%). Ex.12 (2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride Step 2: to a solution of N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]- 2-methylpropane-2-sulfinamide Ex.12a (540 mg, 1.41 mmol) dissolved in MeOH (5 mL) was added conc. HCl (2.7 mL) at 0° C. The reaction mixture was stirred at this temperature for 1 h. The solvent was removed and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride Ex.12 (209 mg, 47%) as white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 2.25 (d, 3H, J = 1.0 Hz), 2.33 (s, 3H), 5.72 (s, 1H), 6.10 (dd, 1H, J = 3.2 Hz, J = 1.1 Hz), 6.26 (d, 1H, J = 3.2 Hz), 7.35 (dd, 1H, J = 8.2 Hz, J = 1.7 Hz), 7.53-7.59 (m, 1H), 7.68 (d, 1H, J = 8.0 Hz), 9.20 (s, 3H).

Intermediate Ex. 13: [4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.31 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.13a 4-methoxy-2-(4-methylpiperidin-1-yl)benzaldehyde Step 1: a solution of 2-bromo-4-methoxybenzaldehyde (1.0 g, 4.65 mmol), 4- methylpiperidine (550 μL, 4.65 mmol), BINAP (116 mg, 0.19 mmol), Pd2(dba)3 (85 mg, 0.09 mmol) and Cs2CO3 (3.78 g, 6.98 mmol) in dry toluene (15 mL) was heated at 110° C. for 18 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure to afford 4-methoxy- 2-(4-methylpiperidin-1-yl)benzaldehyde Ex.13a (1.08 g, 87%). The intermediate was used as such for the next step. Ex.13b N-[[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl]methylidene]-2- methylpropane-2-sulfinamide Step 2: a solution of 4-methoxy-2-(4-methylpiperidin-1-yl)benzaldehyde Ex.13a (942 mg, 4.04 mmol), titanium ethoxide (3.5 g, 16.15 mmol), 2-methyl-propane- sulfinamide (651 mg, 5.37 mmol) in dry THF was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.13c N-{[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl 2-methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (152 mg, 6.25 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (909 mg, 5.65 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[[4-methoxy-2-(4- methylpiperidin-1-yl)phenyl]methylidene]-2-methylpropane-2-sulfinamide Ex.13b (1.0 g, 2.97 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [5:1] as eluent affording N-{[4-methoxy-2-(4-methylpiperidin-1- yl)phenyl](5-methylfuran-2-yl)methyl}-2-methylpropane-2-sulfinamide Ex.13c (540 mg, 43%) as yellowish oil. Ex.13 [4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2- yl)methanamine hydrochloride Step 4: to a solution of N-{[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5- methylfuran-2-yl)methyl}-2-methylpropane-2-sulfinamide Ex.13c (540 mg, 1.29 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (1.5 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford [4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5- methylfuran-2-yl)methanamine hydrochloride Ex.13 (430 mg, 95%) as off-white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 0.97 (d, 3H, J = 6.3 Hz), 1.26-1.56 (m, 4H), 1.58-1.80 (m, 2H), 2.25 (s, 3H), 2.64-3.08 (m, 4H), 3.78 (s, 3H), 5.85 (s, 1H), 6.09 (d, 1H, J = 3.2 Hz), 6.25 (d, 1H, J = 3.2 Hz), 6.79-6.90 (m, 2H), 7.61 (d, 1H, J = 8.6 Hz), 8.90 (br(s), 3H).

Intermediate Ex. 14: {4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.32 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.14a 2-(4-(trifluoromethyl)piperidin-1-yl)-4-methoxybenzaldehyde Step 1: a solution of 2-bromo-4-methoxybenzaldehyde (1.0 g, 4.65 mmol), 4- (trifluoromethyl)piperidine (630 μL, 4.65 mmol), BINAP (116 mg, 0.19 mmol), Pd2(dba)3 (85 mg, 0.09 mmol) and Cs2CO3 (3.78 g, 6.98 mmol) in dry toluene (15 mL) was heated at 110° C. for 18 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of CH2Cl2/EtOAc ([6:4] to [7:3]) followed by hexanes/EtOAc [10:1] to afford 2-(4- (trifluoromethyl)piperidin-1-yl)-4-methoxybenzaldehyde Ex.14a (1.34 g, quantitative). Ex.14b N-[{4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}methylidene]-2- methylpropane-2-sulfinamide Step 2: a solution of 2-(4-(trifluoromethyl)piperidin-1-yl)-4-methoxybenzaldehyde Ex.14a (1.33 g, 4.65 mmol), titanium ethoxide (4.02 g, 18.60 mmol), 2-methyl- propane-sulfinamide (746 mg, 6.18 mmol) in dry THF was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.14c N-({4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl)(5-methylfuran-2- yl)methyl)-2-methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (131 mg, 5.39 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (783 mg, 4.87 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[{4-methoxy-2-[4- (trifluoromethyl)piperidin-1-yl]phenyl}methylidene]-2-methylpropane-2- sulfinamide Ex.14b (1.0 g, 2.56 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [5:1] as eluent affording N-({4-methoxy- 2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methyl)-2- methylpropane-2-sulfinamide Ex.14c (593 mg, 49%) as yellowish oil. Ex.14 {4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2- yl)methanamine hydrochloride Step 4: to a solution of N-({4-methoxy-2-[4-(trifluoromethyl)piperidin-1- yl]phenyl}(5-methylfuran-2-yl)methyl)-2-methylpropane-2-sulfinamide Ex.14c (587 mg, 1.24 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (1.4 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford {4-methoxy-2-[4- (trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methanamine hydrochloride Ex.14 (498 mg, 99%) as off-white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 1.56-1.74 (m, 2H), 1.77-1.99 (m, 2H), 2.25 (s, 3H), 2.55- 2.67 (m, 2H), 2.68-2.94 (m, 2H), 3.02-3.17 (m, 1H), 3.78 (s, 3H), 5.84 (s, 1H), 6.05-6.17 (m, 1H), 6.27 (d, 1H, J = 3.1 Hz), 6.77-6.94 (m, 2H), 7.62 (d, 1H, J = 8.7 Hz), 8.87 (br(s), 3H).

Intermediate Ex. 15: 2-[amino(5-methylfuran-2-yl)methyl]-5-methoxy-N,N-dimethylaniline hydrochloride (FIG. 2B)

TABLE 1.33 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.15a 2-(dimethylamino)-4-methoxybenzaldehyde Step 1: a solution of 2-bromo-4-methoxybenzaldehyde (2.0 g, 9.30 mmol), 2M dimethylamine in THF (11.6 mL, 23.25 mmol), BINAP (232 mg, 0.37 mmol), Pd2(dba)3 (170 mg, 0.19 mmol) and Cs2CO3 (7.56 g, 23.25 mmol) in dry toluene (30 mL) was heated at 110° C. for 3 days. 1N HCl was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was used as such in the next step without further purification. Ex.15b N-[[2-(dimethylamino)-4-methoxyphenyl]methylidene]-2-methylpropane-2- sulfinamide Step 2: a solution of 2-(dimethylamino)-4-methoxybenzaldehyde Ex.15a (1.41 g, 7.87 mmol), titanium ethoxide (3.59 g, 15.73 mmol), 2-methyl-propane- sulfinamide (954 mg, 7.87 mmol) in dry THF was stirred at rt for 3 days. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.15c N-{[2-(dimethylamino)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2- methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (163 mg, 6.71 mmol) in dry THF (small amount) was added cat. amount of iodine followed by 2-bromo-5- methylfurane (1.03 g, 6.37 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[[2-(dimethylamino)-4-methoxyphenyl]methylidene]-2- methylpropane-2-sulfinamide Ex.15b (1.0 g, 3.54 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [7:3] as eluent affording N-{[2-(dimethylamino)-4-methoxyphenyl](5-methylfuran-2- yl)methyl}-2-methylpropane-2-sulfinamide Ex.15c (826 mg, 64%) as yellowish oil. Ex.15 2-[amino(5-methylfuran-2-yl)methyl]-5-methoxy-N,N-dimethylaniline hydrochloride Step 4: to a solution of N-{[2-(dimethylamino)-4-methoxyphenyl](5-methylfuran- 2-yl)methyl}-2-methylpropane-2-sulfinamide Ex.15c (820 mg, 2.25 mmol) dissolved in small amount of dioxane was added 4N HCl in dioxane (1.3 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford 2-[amino(5-methylfuran-2-yl)methyl]-5-methoxy-N,N- dimethylaniline hydrochloride Ex.15 (633 mg, 95%) as off-white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 2.24 (d, 3H, J = 1.0 Hz), 2.83 (s, 6H), 3.82 (s, 3H), 6.10 (dd, 1H, J = 3.2 Hz, J = 1.2 Hz), 6.21 (s, 1H), 6.35 (d, 1H, J = 3.2 Hz), 6.98 (d, 1H, J = 8.7 Hz), 7.11 (s, 1H), 7.66 (d, 1H, J = 8.7 Hz), 9.09 (br(s), 3H).

Intermediate Ex. 16: (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.34 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.16a 2-(3-aza-bicyclo[3.1.0]hexan-3-yl)-4-methoxybenzaldehyde Step 1: a solution of 2-bromo-4-methoxybenzaldehyde (900 mg, 4.19 mmol), 3- aza-bicyclo[3.1.0]hexane hydrochloride (500 mg, 4.19 mmol), BINAP (104 mg, 0.17 mmol), Pd2(dba)3 (77 mg, 0.08 mmol) and Cs2CO3 (3.40 g, 6.29 mmol) in dry toluene (15 mL) was heated at 110° C. for 18 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of CH2Cl2/EtOAc ([6:4] to [7:3]) followed by hexanes/EtOAc [10:1] to afford 2-(3-aza-bicyclo[3.1.0]hexan-3-yl)-4-methoxybenzaldehyde Ex.16a (731 mg, 80%). Ex.16b N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)methylidene]-2- methylpropane-2-sulfinamide Step 2: a solution of 2-(3-aza-bicyclo[3.1.0]hexan-3-yl)-4-methoxybenzaldehyde Ex.16a (731 mg, 3.36 mmol), titanium ethoxide (2.61 g, 13.46 mmol), 2-methyl- propane-sulfinamide (484 mg, 4.47 mmol) in dry THF was stirred at rt for 48 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.16c N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2- yl)methyl]-2-methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (153 mg, 6.29 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (871 mg, 5.41 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[(2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)methylidene]-2-methylpropane-2- sulfinamide Ex.16b (963 mg, 3.00 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [5:1] as eluent affording N-[(2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex..16c (525 mg, 43%) as yellowish oil. Ex.16 (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2- yl)methanamine hydrochloride Step 4: to a solution of N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- methoxyphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2-sulfinamide Ex.16c (525 mg, 1.30 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (1.8 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methanamine hydrochloride Ex.16 (205 mg, 47%) as orange solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 0.50 (dt, 1H, J = 7.6 Hz, J = 4.2 Hz), 0.75 (q, 1H, J = 3.9 Hz), 1.47-1.60 (m, 2H), 2.27 (s, 3H), 2.82 (dd, 1H, J = 8.9 Hz, J = 3.3 Hz), 2.95 (d, 1H, J = 8.9 Hz), 3.08 (d, 1H, J = 8.8 Hz), 3.28 (dd, 1H, J = 8.7 Hz, J = 3.5 Hz), 3.77 (s, 3H), 5.53-5.63 (m, 1H), 6.09 (dd, 1H, J = 3.2 Hz, J = 1.2 Hz), 6.18 (d, 1H, J = 3.2 Hz), 6.77-6.84 (m, 2H), 7.54 (d, 1H, J = 8.3 Hz), 8.84 (br(s), 3H).

Intermediate Ex. 18: [5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.35 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.18a 5-methyl-2-(piperidin-1-yl)benzaldehyde Step 1: a solution of 2-bromo-5-methylbenzaldehyde (1.15 g, 5.78 mmol), piperidine (571 μL, 5.78 mmol), BINAP (144 mg, 0.23 mmol), Pd2(dba)3 (159 mg, 0.17 mmol) and Cs2CO3 (2.81 g, 8.67 mmol) in dry toluene (15 mL) was heated at 110° C. overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material purified by silica gel column chromatography using hexanes/EtOAc [9:1] as eluent affording 5-methyl-2-(piperidin-1-yl)benzaldehyde Ex.18a (1.12 g, 95%). Ex.18b 2-methyl-N-[[5-methyl-2-(piperidin-1-yl)phenyl]methylidene]propane-2- sulfinamide Step 2: a solution of 5-methyl-2-(piperidin-1-yl)benzaldehyde Ex.18a (1.12 g, 5.51 mmol), titanium ethoxide (4.78 g, 22.04 mmol), 2-methyl-propane- sulfinamide (888 mg, 7.33 mmol) in dry THF was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.18c 2-methyl-N-{[5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- yl)methyl}propane-2-sulfinamide Step 3: to a suspension of magnesium powder (253 mg, 10.42 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (1.5 g, 9.32 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared 2-methyl-N-[[5-methyl- 2-(piperidin-1-yl)phenyl]methylidene]propane-2-sulfinamide Ex.18b (1.68 g, 5.48 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [4:1] as eluent affording 2-methyl-N-{[5-methyl-2-(piperidin-1- yl)phenyl](5-methylfuran-2-yl)methyl}propane-2-sulfinamide Ex.18c (1.13 g, 53%) as yellowish oil. Ex.18 [5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methanamine hydrochloride Step 4: to a solution of 2-methyl-N-{[5-methyl-2-(piperidin-1-yl)phenyl](5- methylfuran-2-yl)methyl}propane-2-sulfinamide Ex.18c (1.12 g, 2.88 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (3.2 mL) at 0° C. The reaction mixture was stirred at this temperature for 1 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford [5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- yl)methanamine hydrochloride Ex.18 (924 mg, quantitative) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 1.44-1.72 (m, 6H), 2.26 (s, 3H), 2.31 (s, 3H), 2.69 (s, 4H), 5.95 (s, 1H), 6.07-6.13 (m, 1H), 6.27 (d, 1H, J = 3.2 Hz), 7.24 (s, 2H), 7.49 (s, 1H), 8.92 (s, 3H). Contains 15% dioxane by weight.

Intermediate Ex. 20: (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine (FIG. 2A)

TABLE 1.36 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.20a N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a suspension of magnesium powder (239 mg, 9.79 mmol) in dry THF (small amount) was added dropwise 1-bromo-2,4-dimethylbenzene (1.64 g, 8.86 mmol) diluted in dry THF (20 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, 2-methyl-N-[(5-methylfuran-2- yl)methylidene]propane-2-sulfinamide Ex.11a (995 mg, 4.66 mmol) diluted in THF (10 mL) was added to the solution. The reaction mixture was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of hexanes/EtOAc ([5:1] to [4:1]) to afford N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex.20a (1.27 g, 85%) as yellowish oil. Ex.20 (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine Step 3: to a solution of N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex.20a (683 mg, 2.14 mmol) dissolved in dry dioxane (5 mL) was added 4N HCl in dioxane (2.4 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine Ex.20 (194 mg, 36%) as white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 2.24 (s, 3H); 2.29 (d, J = 4.7 Hz, 6H), 5.64 (s, 1H), 6.02-6.19 (m, 1H), 6.25 (d, 1H, J = 3.2 Hz), 7.09-7.16 (m, 1H), 7.44 (d, 1H, J = 8.0 Hz), 8.96 (s, 3H).

Intermediate Ex. 21: (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl) methanamine hydrochloride (FIG. 2B)

TABLE 1.37 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.21a 2-(3-aza-bicyclo[3.1.0]hexan-3-yl)-4-methylbenzaldehyde Step 1: a solution of 2-bromo-4-methylbenzaldehyde (500 mg, 2.51 mmol), 3- aza-bicyclo[3.1.0]hexane hydrochloride (451 mg, 3.77 mmol), BINAP (63 mg, 0.10 mmol), Pd2(dba)3 (46 mg, 0.05 mmol) and Cs2CO3 (2.04 g, 6.28 mmol) in dry toluene (15 mL) was heated at 110° C. for 18 h. 1N HCl was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was used as such in the next step. Ex.21b N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)methylidene]-2- methylpropane-2-sulfinamide Step 2: a solution of 2-(3-aza-bicyclo[3.1.0]hexan-3-yl)-4-methylbenzaldehyde Ex.21a (477 mg, 2.37 mmol), titanium ethoxide (1.08 g, 4.74 mmol), 2-methyl- propane-sulfinamide (287 mg, 2.37 mmol) in dry THF was stirred at rt for 48 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.21c N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2- methylpropane-2-sulfinamide Step 3: to a solution of N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Ex.21b (720 mg, 2.36 mmol) in dry THF (10 mL) was added phenylmagnesium bromide 1M solution in THF (7.10 mL, 7.08 mmol) at rt. The reaction mixture was stirred at that temperature for 16 h. Sat. NH4Cl was added to quench the reaction. The aqueous layer was extracted with EtOAc. The organic layer was dried over MgSO4, filtered and the solution was concentrated to dryness. The crude material was purified by silica gel column chromatography eluting with a gradient of hexanes/EtOAc ([4:1] to [3:1]) affording N-[(2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2-methylpropane- 2-sulfinamide Ex.21c (677 mg, 75%). Ex.21 (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methanamine hydrochloride Step 4: to a solution of N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- methylphenyl)(phenyl)methyl]-2-methylpropane-2-sulfinamide Ex.21c (674 mg, 1.76 mmol) dissolved in small amount of dioxane was added 4N HCl in dioxane (1.0 mL) at rt. The reaction mixture was stirred at this temperature for 2 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- methylphenyl)(phenyl)methanamine hydrochloride Ex.21 (449 mg, 81%) as off- white solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 0.47 (dt, 1H, J = 7.5 Hz, J = 4.1 Hz), 0.74 (d, 1H, J = 4.1 Hz), 1.41-1.49 (m, 1H), 1.49-1.60 (m, 1H), 2.29 (s, 3H), 2.69 (d, 1H, J = 8.7 Hz), 2.89 (d, 1H, J = 8.0 Hz), 3.12 (d, 1H, J = 8.2 Hz), 3.18 (d, 1H, J = 8.8 Hz), 5.76 (s, 1H), 7.05 (d, 1H, J = 8.0 Hz), 7.18 (s, 1H), 7.31-7.37 (m, 1H), 7.40 (m, 2H), 7.41 (s, 2H), 7.53 (d, 1H, J = 7.9 Hz), 9.02 (s, 3H).

Intermediate Ex. 25: (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.38 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.25a N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2- yl)methyl]-2-methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (136 mg, 5.59 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (846 mg, 4.45 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[(2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)methylidene]-2-methylpropane-2- sulfinamide Ex.21b (1.0 g, 3.28 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt for 48 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [4:1] as eluent affording N-[(2-{3- azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex.25a (330 mg, 26%) as yellowish oil. Ex.25 (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2- yl)methanamine hydrochloride Step 4: to a solution of N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5- methylfuran-2-yl)methyl]-2-methylpropane-2-sulfinamide Ex.25a (330 mg, 0.85 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (600 μL) at 0° C. The reaction mixture was stirred at this temperature for 30 min and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride Ex.25 (229 mg, 84%) as yellow solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 0.50 (td, 1H, J = 7.6 Hz, J = 4.2 Hz), 0.76 (q, 1H, J = 4.0 Hz), 1.45-1.61 (m, 2H), 2.26 (s, 3H), 2.30 (s, 3H), 2.82 (dd, 1H, J = 9.0 Hz, J = 3.4 Hz), 2.91 (d, 1H, J = 8.9 Hz), 3.07 (d, 1H, J = 8.7 Hz), 3.27 (dd, 1H, J = 8.7 Hz, J = 3.5 Hz), 5.64 (d, 1H, J = 5.5 Hz), 6.09 (dd, 1H, J = 3.1 Hz, J = 1.2 Hz), 6.18 (d, 1H, J = 3.2 Hz), 7.03 (dd, 1H, J = 8.1 Hz, J = 1.6 Hz), 7.14 (d, 1H, J = 1.6 Hz), 7.50 (d, 1H, J = 7.9 Hz), 8.87 (s, 3H).

Intermediate Ex. 34: (4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride (FIG. 2B)

TABLE 1.39 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.34a N-[(4-methoxy-2-methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Step 1: a solution of 4-methoxy-2-methylbenzaldehyde (1.0 g, 6.66 mmol), titanium ethoxide (5.78 g, 26.63 mmol), 2-methyl-propane-sulfinamide (1.07 g, 8.86 mmol) in dry THF was stirred at rt for 48 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.34b N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane- 2-sulfinamide Step 2: to a suspension of magnesium powder (182 mg, 7.48 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (1.14 g, 7.10 mmol) diluted in dry THF (10 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-[(4-methoxy-2- methylphenyl)methylidene]-2-methylpropane-2-sulfinamide (1.0 g, 3.95 mmol) diluted in THF (10 mL) was added to the solution at 0° C. The reaction mixture was then stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc [4:1] as eluent affording N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2- yl)methyl]-2-methylpropane-2-sulfinamide Ex.34b (887 mg, 67%) as yellowish oil. Ex.34 (4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methanamine hydrochloride Step 3: to a solution of N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2- yl)methyl]-2-methylpropane-2-sulfinamide Ex.34b (886 mg, 2.64 mmol) dissolved in small amount of Et2O was added 4N HCl in dioxane (3.0 mL) at 0° C. The reaction mixture was stirred at this temperature for 1 h and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight to afford (4-methoxy-2-methylphenyl)(5-methylfuran-2- yl)methanamine hydrochloride Ex.34 (410 mg, 58%) as yellowish solid. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 2.24 (s, 3H), 2.32 (s, 3H), 3.76 (s, 3H), 5.60 (s, 1H), 6.07-6.10 (m, 1H), 6.27 (d, 1H, J = 3.2 Hz), 6.84 (d, 1H, J = 2.7 Hz), 6.88 (dd, 1H, J = 8.6 Hz, J = 2.8 Hz), 7.48 (d, 1H, J = 8.6 Hz), 8.97 (br(s), 3H).

Intermediate Ex. 35: [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methanamine (FIG. 2B)

TABLE 1.40 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.35a 2-(azepan-1-yl)-4-methoxybenzaldehyde Step 1: a solution of 2-bromo-4-methoxybenzaldehyde (0.5 g, 2.33 mmol), hexamethyleneimine (262 μL, 2.33 mmol), BINAP (58 mg, 0.10 mmol), Pd2(dba)3 (43 mg, 0.05 mmol) and Cs2CO3 (1.134 g, 3.48 mmol) in dry toluene (15 mL) was heated at 95° C. for 17 h. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using hexanes/EtOAc as eluent ([100:1] to [20:1]) to afford 2-(azepan-1-yl)-4-methoxybenzaldehyde Ex.35a (526 mg, 96%). Ex.35b N-{[2-(azepan-1-yl)-4-methoxyphenyl]methylidene}-2-methylpropane-2- sulfinamide Step 2: a solution of 2-(azepan-1-yl)-4-methoxybenzaldehyde Ex.35a (526 mg, 2.25 mmol), titanium ethoxide (1.9 mL, 9.02 mmol), (R)-2-methyl-propane- sulfinamide (276 mg, 2.48 mmol) in dry THF was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was pure enough and used in the next step without further purification. Ex.35c N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2- methylpropane-2-sulfinamide Step 3: to a suspension of magnesium powder (60 mg, 2.46 mmol) in dry THF (small amount) was added dropwise 2-bromo-5-methylfurane (377 mg, 2.34 mmol) diluted in dry THF (5 mL) and the reaction was heated at 40° C. After completion of Grignard reagent, the previously prepared N-{[2-(azepan-1-yl)-4- methoxyphenyl]methylidene}-2-methylpropane-2-sulfinamide Ex.35b (394 mg, 1.17 mmol diluted in THF (5 mL) was added to the solution. The reaction mixture was stirred at rt overnight. Water was added to quench the reaction. The two layers were partitionated and the organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using a gradient of hexanes/EtOAc to afford N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2- yl)methyl}-2-methylpropane-2-sulfinamide Ex.35c (283 mg, 60%) as yellowish oil. Ex.35 [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methanamine Step 4: to a solution of N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2- yl)methyl}-2-methylpropane-2-sulfinamide Ex.35c (283 mg, 0.70 mmol) in MeOH (5 mL) was added conc. HCl (3.1 mL) at 0° C. The reaction mixture was stirred at this temperature for 2 h and then quench with sat. NaHCO3 to reach pH 7-8. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography using CH2Cl2/EtOAc as eluent ([10:0] to [8:2]) followed by flash silica gel column chromatography using hexanes/EtOAc as eluent to afford [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methanamine Ex.35 (62 mg, 28%) as yellowish oil. 1H NMR (400 MHz, DMSO-d6, δ in ppm): 1.66 (s, 8H), 2.17 (s, 3H), 2.91-3.06 (m, 4H), 3.71 (s, 3H), 5.41 (s, 1H), 5.92 (s, 2H), 6.62 (dd, 1H, J = 8.5 Hz, J = 2.6 Hz), 6.66 (d, 1H, J = 2.6 Hz), 7.23 (d, 1H, J = 8.5 Hz) (NH2 exchange with deuterated solvent).

Intermediate Ex. 38: (4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methanamine (FIG. 2B)

TABLE 1.41 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.38a N-[(4-chloro-2-methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Step 1: 4-chloro-2-methylbenzaldehyde (2.0 g, 12.94 mmol) was dissolved in dry THF (15 mL). Titanium ethoxide (5.43 mL, 25.87 mmol) and 2-methyl-2- propane-sulfinamide (1.65 g, 13.58 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Sat. NH4Cl was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with Cyclohexane/EtOAc (90:10) to afford N-[(4-chloro-2-methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Ex.38a (1.82 g, 55%) as colorless oil which crystallizes to white solid. Ex.38b N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a solution of 2-bromo-5-methylfuran (637 mg, 3.96 mmol) diluted in dry THF (13 mL) was added dropwise nBuLi (2.68 mL, 4.29 mmol) at −78° C. and under N2 atmosphere. After 5 min, N-[(4-chloro-2-methylphenyl)methylidene]-2- methylpropane-2-sulfinamide Ex.38a (850 mg, 3.30 mmol) dissolved in dry THF (8 mL) was added dropwise to the mixture. After completion of the reaction, sat. NH4Cl was added at 0° C. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using Cyclohexane/EtOAc (50:50) as eluent to afford N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex.38b (645 mg, 58%) as pale yellow oil. Ex.38 (4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methanamine Step 3: to a solution of N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]- 2-methylpropane-2-sulfinamide Ex.38b (645 mg, 1.90 mmol) dissolved in small amount of Et2O was added a saturated solution of HCl in Et2O at 0° C. The solution was stirred at this temperature until completion of the reaction and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight. The crude material was purified by preparative HPLC to afford (4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methanamine Ex.38 (121 mg, 27%) as yellow oil. 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.16 (s, 3H), 2.28 (s, 3H), 5.12 (s, 1H), 5.93 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 5.96 (d, 1H, J = 3.2 Hz), 7.20-7.23 (m, 2H), 7.37 (d, 1H, J = 9.0 Hz).

Intermediate Ex. 39: (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine (FIG. 2B)

TABLE 1.42 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.39a N-[(2,4-dichlorophenyl)methylidene]-2-methylpropane-2-sulfinamide Step 1: 2,4-dichlorobenzaldehyde (2.0 g, 11.43 mmol) was dissolved in dry THF (15 mL). Titanium ethoxide (4.79 mL, 22.86 mmol) and 2-methyl-2-propane- sulfinamide (1.45 g, 12.00 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Sat. NH4Cl was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with Cyclohexane/EtOAc (90:10) to afford N-[(2,4-dichlorophenyl)methylidene]-2-methylpropane-2-sulfinamide Ex.39a (2.12 g, 67%) as pale yellow solid. Ex.39b -[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a solution of 2-bromo-5-methylfuran (556 mg, 3.45 mmol) diluted in dry THF (5 mL) was added dropwise nBuLi (2.34 mL, 3.74 mmol) at −78° C. and under N2 atmosphere. After 5 min, N-[(2,4-dichlorophenyl)methylidene]-2- methylpropane-2-sulfinamide Ex.39a (800 mg, 2.88 mmol) dissolved in dry THF (8 mL) was added dropwise to the mixture. The solution was stirred at −78° C. for 30 min. Sat. NH4Cl was added at 0° C. to quench the reaction. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using Cyclohexane/EtOAc (50:50) as eluent to afford N-[(2,4-dichlorophenyl)(5- methylfuran-2-yl)methyl]-2-methylpropane-2-sulfinamide Ex.39b (700 mg, 68%) as pale yellow oil. Ex.39 (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine Step 3: to a solution of N-[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-2- methylpropane-2-sulfinamide Ex.39b (700 mg, 1.94 mmol) diluted in small amount of Et2O was added a saturated solution of HCl in Et2O at 0° C. The solution was stirred at this temperature until completion of the reaction and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight. The crude material was purified by preparative HPLC to afford (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine Ex.39 (144 mg, 29%) as yellow oil. 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.17 (s, 3H), 2.6-2.78 (m, 2H), 5.30 (s, 1H), 5.93-5.96 (m, 2H), 7.44 (dd, 1H, J = 8.7 Hz, J = 2.4 Hz), 7.55 (d, 1H, J = 2.1 Hz), 7.61 (d, 1H, J = 8.4 Hz).

Intermediate Ex. 40: (2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methanamine (FIG. 2B)

TABLE 1.43 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.40a N-[(2-chloro-4-methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Step 1: 2-chloro-4-methylbenzaldehyde (2.0 g, 12.94 mmol) was dissolved in dry THF (15 mL). Titanium ethoxide (5.43 mL, 25.87 mmol) and 2-methyl-2- propane-sulfinamide (1.65 g, 13.58 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Sat. NH4Cl was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with Cyclohexane/EtOAc (90:10) to afford N-[(2-chloro-4-methylphenyl)methylidene]-2-methylpropane-2-sulfinamide Ex.40a (1.80 g, 54%) as white solid. Ex.40b N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a solution of 2-bromo-5-methylfuran (562 mg, 3.49 mmol) diluted in dry THF (5 mL) was added dropwise nBuLi (2.36 mL, 3.78 mmol) at −78° C. and under N2 atmosphere. After 5 min, N-[(2-chloro-4-methylphenyl)methylidene]-2- methylpropane-2-sulfinamide Ex.40a (750 mg, 2.91 mmol) dissolved in dry THF (8 mL) was added dropwise to the mixture. The solution was stirred at −78° C. for 30 min. Sat. NH4Cl was added at 0° C. to quench the reaction. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using Cyclohexane/EtOAc (50:50) as eluent to afford N-[(2-chloro-4-methylphenyl)(5- methylfuran-2-yl)methyl]-2-methylpropane-2-sulfinamide Ex.40b (640 mg, 65%) as pale yellow oil. Ex.40 (2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methanamine Step 3: to a solution of N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]- 2-methylpropane-2-sulfinamide Ex.40b (640 mg, 1.88 mmol) diluted in small amount of Et2O was added a saturated solution of HCl in Et2O at 0° C. The solution was stirred at this temperature until completion of the reaction and then the solid was collected by filtration. The solid was triturated with Et2O and dried until constant weight. The crude material was purified by preparative HPLC to afford (2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methanamine Ex.40 (146 mg, 33%) as yellow oil 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.17 (s, 3H), 2.27 (s, 3H), 2.36-2.47 (m, 2H), 5.27 (s, 1H), 5.92-5.93 (m, 2H), 7.12-7.15 (m, 1H), 7.20-7.22 (m, 1H), 7.42 (d, 1H, J = 7.8 Hz).

Intermediate Ex. 47: (5-chlorofuran-2-yl)(2,4-dimethylphenyl)methanamine (FIG. 2A)

TABLE 1.44 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.47a N-[(5-chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Step 1: 5-chlorofuran-2-carbaldehyde (5.0 g, 38.31 mmol) was dissolved in dry THF (50 mL). Titanium ethoxide (9.64 mL, 45.97 mmol) and 2-methyl-2- propane-sulfinamide (4.88 g, 40.22 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Sat. NH4Cl was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with Cyclohexane/EtOAc (85:15) to afford N-[(5-chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Ex.47a (8.86 g, 99%) as yellow oil. Ex.47b N-[(5-chlorofuran-2-yl)(2,4-dimethylphenyl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a solution of bromo(2,4-dimethylphenyl)magnesium 0.5M in THF (17.12 mL, 8.56 mmol) was added dropwise at −78° C. and under N2 atmosphere N-[(5-chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Ex.47a (2.00 g, 8.56 mmol) diluted in dry THF (15 mL). The reaction mixture was slowly warmed to rt. Sat. NH4Cl was added to quench the reaction. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using Cyclohexane/EtOAc (80:20) as eluent to give N-[(5-chlorofuran-2-yl)(2,4- dimethylphenyl)methyl]-2-methylpropane-2-sulfinamide Ex.47b (500 mg, 17%) as colorless oil. Ex.47 (5-chlorofuran-2-yl)(2,4-dimethylphenyl)methanamine Step 3: to a solution of N-[(5-chlorofuran-2-yl)(2,4-dimethylphenyl)methyl]-2- methylpropane-2-sulfinamide Ex.47b (495 mg, 1.46 mmol) diluted in dioxane (6 mL) was added at 0° C. HCl 4M in dioxane (1.64 mL, 6.55 mmol). The solution was stirred at this temperature until completion of the reaction. Water was added to quench the reaction and the aqueous solution was extracted twice with CH2Cl2. The two phases were partitionated. The aqueous layer was basified with NaOH 5M up pH = 10 was reached. The aqueous solution was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated to dryness to afford (5-chlorofuran-2-yl)(2,4- dimethylphenyl)methanamine Ex.47 (313 mg, 91%) as yellow solid. 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.23 (s, 3H), 2.25 (s, 3H), 2.27-2.39 (br(s), 2H), 5.11 (s, 1H), 6.20 (dd, 1H, J = 3.3 Hz, J = 0.9 Hz), 6.33 (d, 1H, J = 3.3 Hz), 6.92-7.01 (m, 2H), 7.19 (d, 1H, J = 7.7 Hz).

Intermediate Ex. 48: (5-chlorofuran-2-yl)(4-methylphenyl)methanamine hydrochloride (FIG. 2A)

TABLE 1.45 Starting compounds, Reaction conditions and Yield, Appearance, ¹H NMR (solvent) Cpd. purification, data Ex.48a N-[(5-chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Step 1: 5-chlorofuran-2-carbaldehyde (5.0 g, 38.31 mmol) was dissolved in dry THF (50 mL). Titanium ethoxide (9.64 mL, 45.97 mmol) and 2-methyl-2- propane-sulfinamide (4.88 g, 40.22 mmol) were added to the reaction mixture. The solution was stirred at rt until completion of the reaction. Sat. NH4Cl was added to quench the reaction and the solution was stirred vigorously. EtOAc was added and the resulting mixture was filtered on Celite. The two layers were partitionated. The organic layer was dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with Cyclohexane/EtOAc (85:15) to afford N-[(5-chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Ex.48a (8.86 g, 99%) as yellow oil. Ex.48b N-[(5-chlorofuran-2-yl)(4-methylphenyl)methyl]-2-methylpropane-2- sulfinamide Step 2: to a solution of bromo(4-methylphenyl)magnesium 1M in THF (8.56 mL, 8.56 mmol) was added dropwise at −78° C. and under N2 atmosphere N-[(5- chlorofuran-2-yl)methylidene]-2-methylpropane-2-sulfinamide Ex.48a (2.00 g, 8.56 mmol) diluted in dry THF (15 mL). The reaction mixture was slowly warmed to rt. Sat. NH4Cl was added to quench the reaction. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered and the solution was concentrated under reduced pressure. The crude material was purified by silica gel column chromatography using Cyclohexane/EtOAc (80:20) as eluent to give N-[(5-chlorofuran-2-yl)(4- methylphenyl)methyl]-2-methylpropane-2-sulfinamide Ex.48b (1.45 g, 52%) as colorless oil which crystallizes to white solid. Ex.48 (5-chlorofuran-2-yl)(4-methylphenyl)methanamine hydrochloride Step 3: to a solution of N-[(5-chlorofuran-2-yl)(4-methylphenyl)methyl]-2- methylpropane-2-sulfinamide Ex.48b (580 mg, 1.78 mmol) diluted in dioxane (7 mL) was added at 0° C. HCl 4M in dioxane (2.00 mL, 8.01 mmol). The solution was stirred at this temperature until completion of the reaction. The precipitate formed was collected by filtration, washed with small amount of dry dioxane and dried until constant weight to afford (5-chlorofuran-2-yl)(4- methylphenyl)methanamine hydrochloride Ex.48 (425 mg, 93%) as white solid. 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.31 (s, 3H), 5.66 (s, 1H), 6.51 (d, 1H, J = 3.4 Hz), 6.54 (d, 1H, J = 3.3 Hz), 7.26 (d, 2H, J = 7.9 Hz), 7.42 (d, 2H, J = 8.1 Hz), 9.17 (br(s), 3H).

Example 2: Synthesis of the Compounds According to the Invention

Protocol A: to a solution of the substituted acid in DMF (0.25 mmol/mL) were added DMAP (2 to 4 equiv), EDCl.HCl (1 to 1.5 equiv) and the substituted amine (1 equiv). The reaction mixture was stirred at rt. After completion of the reaction (monitored by TLC), sat. NH4Cl or HCl 0.5N was added and the solution was extracted with EtOAc. The organic layer was washed with sat. NH4Cl, dried over MgSO4, filtered and evaporated to dryness under reduced pressure.

TABLE 2 All the NMR were performed in DMSO-d6 Starting compounds, Reaction conditions and purification Yield, MP, Appearance, ¹H NMR (solvent) data, Cpd. Mass (ES+ or ES−) data  1 2-[4-(1,1-dioxo-1- From phenyl[2-(piperidin-1-yl)phenyl]methanamine Ex.2 thiomorpholin-4- and 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetic Ex.1 yl)phenyl]-N- acid following protocol A, DMAP (2.2 equiv), EDCl•HCl (1.1 {phenyl[2- equiv), 2 h at rt, the crude material was triturated in Et2O (piperidin-1- containing small amount of CH2Cl2 and filtered-off, yield yl)phenyl]methyl} 61%, mp: 202° C., appearance: white solid acetamide 1H NMR (300 MHz, δ in ppm): 1.44-1.58 (m, 6H), 2.47-2.52 (m, 2H), 2.84-2.88 (m, 2H), 3.06-3.09 (m, 4H), 3.42 (s, 2H), 3.70-3.73 (m, 4H), 6.59 (d, 1H, J = 8.6 Hz), 6.93 (d, 2H, J = 8.8 Hz), 7.02-7.08 (m, 1H), 7.12-7.28 (m, 10H), 8.70 (d, 1H, J = 8.6 Hz); m/z: 518 [M + H]+ (calc. mass: 517).  2 2-[5-(1,1-dioxo-1- From phenyl[2-(piperidin-1-yl)phenyl]methanamine Ex.2 thiomorpholin-4- and 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- yl)-2- methylphenyl]acetic acid Ex.3 following protocol A, DMAP methylphenyl]-N- (2.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, the crude {phenyl[2- material was triturated in EtOAc and filtered-off, yield 22%, (piperidin-1- mp: 188° C., appearance: white solid yl)phenyl]methyl} 1H NMR (300 MHz, δ in ppm): 1.47-1.59 (m, 6H), 2.15 (s, acetamide 3H), 2.48-2.50 (m, 2H), 2.86-2.89 (m, 2H), 3.07-3.09 (m, 4H), 3.52 (s, 2H), 3.63-3.65 (m, 4H), 6.65 (d, 1H, J = 8.7 Hz), 6.79 (dd, 1H, J = 2.6 Hz, J = 8.3 Hz), 6.92 (d, 1H, J = 2.6 Hz), 7.00 (d, 1H, J = 8.4 Hz), 7.07-7.23 (m, 6H), 7.26-7.34 (m, 3H), 8.76 (d, 1H, J = 8.7 Hz); m/z: 532 [M + H]+ (calc. mass: 531).″  3 2-[5-(1,1-dioxo-1- From phenyl[2-(piperidin-1-yl)phenyl]methanamine Ex.2 thiomorpholin-4- and 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- yl)-2- fluorophenyl]acetic acid Ex.4 following protocol A, DMAP fluorophenyl]-N- (2.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, the crude {phenyl[2- material was triturated in EtOAc and filtered-off, yield 43%, (piperidin-1- mp: 184° C., appearance: white solid yl)phenylymethyl} 1H NMR (300 MHz, δ in ppm): 1.48-1.59 (m, 6H), 2.50-2.54 acetamide (m, 2H), 2.88-2.92 (m, 2H), 3.12-3.13 (m, 4H), 3.56 (s, 2H), 3.61-3.65 (m, 4H), 6.65 (d, 1H, J = 8.6 Hz), 6.89-6.94 (m, 1H), 6.97-7.06 (m, 2H), 7.07-7.13 (m, 1H), 7.15-7.23 (m, 5H), 7.27-7.33 (m, 3H), 8.85 (d, 1H, J = 8.7 Hz); m/z: 536 [M + H]+ (calc. mass: 535).  4 2-[5-(1,1-dioxo-1- From [4-methyl-2-(morpholin-4- thiomorpholin-4- yl)phenyl](phenyl)methanamine Ex.5 and 2-[5-(1,1-dioxo-1- yl)-2- thiomorpholin-4-yl)-2-fluorophenyl]acetic acid Ex.4 following fluorophenyl]-N- protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at {[4-methyl-2- rt, the crude material was triturated in EtOAc and filtered- (morpholin-4- off, yield 70%, mp: 207° C., appearance: white solid yl)phenyl](phenyl) 1H NMR (300 MHz, δ in ppm): 2.26 (s, 3H), 2.52-2.56 (m, methyl}acetamide 2H), 2.89-2.94 (m, 2H), 3.09-3.12 (m, 4H), 3.53-3.67 (m, 10H), 6.62 (d, 1H, J = 8.7 Hz), 6.91-7.04 (m, 5H), 7.15-7.21 (m, 4H), 7.26-7.31 (m, 2H), 8.83 (d, 1H); m/z: 552 [M + H]+ (calc. mass: 551).  5 2-[5-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[5-(1,1-dioxo-1-thiomorpholin- yl)-2- 4-methylphenyl]acetic acid Ex.3 following protocol A, methylphenyl]-N- substituted amine (0.9 equiv), DMAP (3.2 equiv), EDCl•HCl {[4-methyl-2- 1.2 equiv), 20 h at rt, purification by column (piperidin-1- chromatography on silica gel (cyclohexane/EtOAc, 60:40), yl)phenyl](5- yield 44%, mp: 101° C., appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 1.42-1.61 (m, 6H), 2.14 (s, yl)methyl}acetamide 3H), 2.19 (s, 3H), 2.26 (s, 3H), 2.54-2.61 (m, 2H), 2.74-2.83 m, 2H), 3.02-3.10 (m, 4H), 3.45 (s, 2H), 3.61-3.69 (m, 4H), 5.82 (d, 1H, J = 3.0 Hz), 5.94 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.52 (d, 1H, J = 8.4 Hz), 6.78 (dd, 1H, J = 8.2 Hz, J = 2.6 Hz), 6.87-6.94 (m, 2H), 6.95 (s, 1H), 6.99 (d, 1H, J = 8.3 Hz), 7.23 (d, 1H, J = 7.7 Hz), 8.70 (d, 1H, J = 8.6 Hz); m/z: 550 [M + H]+ (calc. mass: 549).  6 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-{[4- 4-yl)phenyl]acetic acid Ex.1 following protocol A, methyl-2- substituted amine (0.9 equiv), DMAP (3.2 equiv), EDCl•HCl (piperidin-1- (1.2 equiv), 20 h at rt, purification by column yl)phenyl](5- chromatography on silica gel (cyclohexane/EtOAc, 60:40), methylfuran-2- yield 44%, mp: 101° C., appearance: white solid yl)methyl}acetamide 1H NMR (300 MHz, δ in ppm): 1.39-1.63 (m, 6H), 2.18 (s, 3H), 2.26 (s, 3H), 2.53-2.60 (m, 2H), 2.73-2.83 (m, 2H), 3.05-3.12 (m, 4H), 3.37 (s, 2H), 3.68-3.77 (m, 4H), 5.80 (d, 1H, J = 2.6 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.47 (d, 1H, J = 8.3 Hz), 6.86 (d, 1H, J = 8.3 Hz), 6.91-6.97 (m, 3H), 7.12 (d, 2H, J = 8.7 Hz), 7.17 (d, 1H, J = 7.8 Hz), 8.67 (d, 1H, J = 8.4 Hz); m/z: 536 [M + H]+ (calc. mass: 535).  7 2-[5-(1,1-dioxo-1- From [4-methyl-2-(morpholin-4- thiomorpholin-4- yl)phenyl](phenyl)methanamine Ex.5 and 2-[5-(1,1-dioxo-1- yl)-2- thiomorpholin-4-yl)-2-methylphenyl]acetic acid Ex.3 methylphenyl]-N- following protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 {[4-methyl-2- equiv), 16 h at rt, the crude material was triturated in EtOAc (morpholin-4- and filtered-off, yield 33%, mp: 219° C., appearance: white yl)phenyl](phenyl) solid methyl}acetamide 1H NMR (300 MHz, δ in ppm): 2.14 (s, 3H), 2.26 (s, 3H), 2.48-2.50 (m, 2H), 2.85-2.90 (m, 2H), 3.03-3.07 (m, 4H), 3.49 (s, 2H), 3.51-3.57 (m, 2H), 3.61-3.65 (m, 6H), 6.61 (d, 1H, J = 8.7 Hz), 6.78 (dd, 1H, J = 2.6 Hz, J = 8.3 Hz), 6.90 (d, 1H, J = 2.6 Hz), 6.94 (d, 1H, J = 7.9 Hz), 6.98-7.00 (m, 2H), 7.16- 7.20 (m, 4H), 7.25-7.30 (m, 2H), 8.72 (d, 1H, J = 8.8 Hz); m/z: 548 [M + H]+ (calc. mass: 547).  8 2-[2-fluoro-5- From [4-methyl-2-(piperidin-1- (morpholin-4- yl)phenyl](phenyl)methanamine Ex.8 and 2-[2-fluoro-5- yl)phenyl]-N-{[4- (morpholin-4-yl)phenyl]acetic acid Ex.7 following protocol A, methyl-2- substituted amine (0.9 equiv), DMAP (3.2 equiv), EDCl•HCl (piperidin-1- (1.2 equiv), 20 h at rt, purification by preparative HPLC, yield yl)phenyl](phenyl) 27%, mp: 82° C., appearance: white solid methyl}acetamide 1H NMR (300 MHz, δ in ppm): 1.40-1.64 (m, 6H), 2.24 (s, 3H), 2.50-2.59 (m, 2H), 2.81-2.91 (m, 2H), 2.94 (t, 4H, J = 4.8 Hz), 3.53 (s, 2H), 3.70 (t, 4H, J = 4.7 Hz), 6.58 (d, 1H, J = 8.7 Hz), 6.76-6.86 (m, 2H), 6.88 (d, 1H, J = 6.8 Hz), 6.93- 7.03 (m, 2H), 7.14-7.22 (m, 4H), 7.22-7.30 (m, 2H), 8.79 (d, 1H, J = 8.6 Hz); m/z: 502 [M + H]+ (calc. mass: 501).  9 N-[(2-bromo-4- From (2-bromo-4-methylphenyl)(phenyl)methanamine Ex.9 methylphenyl) and 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetic acid (phenyl)methyl]-2-[4- Ex.1 following protocol A, DMAP (2.2 equiv), EDCl•HCl (1.1 (1,1-dioxo-1- equiv), 20 h at rt, purification by preparative HPLC, yield thiomorpholin-4- 17%, mp: 142° C., appearance: white solid yl)phenyl]acetamide 1H NMR (300 MHz, δ in ppm): 2.27 (s, 3H), 3.04-3.13 (m, 4H), 3.41 (s, 2H), 3.67-3.77 (m, 4H), 6.30 (d, 1H, J8.1 Hz), 6.95 (d, 2H, J = 8.8 Hz), 7.09-7.22 (m, 5H), 7.23-7.35 (m, 4H), 7.43 (d, 1H, J = 0.8 Hz), 8.93 (d, 1H, J = 8.2 Hz); m/z: 527 [M + H]+, 529 [M + H]+ (calc. mass: 526). 10 2-[4-(1,1-dioxo-1- From [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.11 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)-3- 4-yl)-3-methylphenyl]acetic acid Ex.10 following protocol A, methylphenyl]-N- DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, {[4-methyl-2- purification by column chromatography on silica gel (trifluoromethyl) (CH2Cl2/MeOH, 98:2), yield 59%, mp: 99° C., appearance: phenyl](5- white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 2.19 (s, 3H), 2.22 (s, 3H), yl)methyl}acetamide 2.37 (s, 3H), 3.23 (br(s), 8H), 3.39 (s, 2H), 5.75 (d, 1H, J = 3.1 Hz), 5.95 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.31 (d, 1H, J = 7.8 Hz), 7.01-7.03 (m, 3H), 7.50-7.59 (m, 3H), 9.07 (d, 1H, J = 8.0 Hz); m/z: 535 [M + H]+ (calc. mass: 534). 11 N-[(2-bromo-4- From (2-bromo-4-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.12 and 2-[4-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)-3-methylphenyl]acetic acid Ex.10 following protocol A, yl)methyl]-2-[4- DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, (1,1-dioxo-1- purification by column chromatography on silica gel thiomorpholin-4- (CH2Cl2/MeOH, 98:2), yield 81%, mp: 110° C., appearance: yl)-3- white solid methylphenyl] 1H NMR (300 MHz, δ in ppm): 2.21 (s, 3H), 2.23 (s, 3H), acetamide 2.28 (s, 3H), 3.24 (br(s), 8H), 3.41 (s, 2H), 5.77 (d, 1H, J = 3.1 Hz), 5.97 (dd, 1H, J = 3 Hz, J = 1.0 Hz), 6.25 (d, 1H, J = 8.1 Hz), 7.02 (d, 2H, J = 1.2 Hz), 7.06 (s, 1H), 7.21 (dd, 1H, J = 7.7 Hz, J = 1.0 Hz), 7.32 (d, 1H, J = 7.9 Hz), 7.43 (d, 1H, J = 0.8 Hz), 9.06 (d, 1H, J = 8.2 Hz); m/z: 545 [M + H]+, 547 [M + H]+ (calc. mass: 544).″ 12 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)-3- 4-yl)-3-methylphenyl]acetic acid Ex.10 following protocol A, methylphenyl]-N- DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, {[4-methyl-2- purification by column chromatography on silica gel (piperidin-1- (Cyclohexane/EtOAc, 50:50), yield 46%, mp: 97° C., yl)phenyl](5- appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 1.45-1.54 (m, 6H), 2.17 (s, yl)methyl}acetamide 3H), 2.22 (s, 3H), 2.25 (s, 3H), 2.53-2.58 (m, 2H), 2.76-2.80 (m, 2H), 3.23 (br(s), 8H), 3.37 (s, 2H), 5.81 (d, 1H, J = 3.1 Hz), 5.92 (dd, 1H, J = 3 Hz, J = 1.0 Hz), 6.48 (d, 1H, J = 8.3 Hz), 6.89 (d, 1H, J = 8.0 Hz), 6.94 (s, 1H), 7.01 (d, 2H, J = 1.1 Hz), 7.04 (s, 1H), 7.19 (d, 1H, J = 7.8 Hz), 8.70 (d, 1H, J = 8.5 Hz); m/z: 550 [M + H]+ (calc. mass: 549). 13 2-[4-(1,1-dioxo-1- From [4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5- thiomorpholin-4- methylfuran-2-yl)methanamine Ex.13 and 2-[4-(1,1-dioxo-1- yl)-3- thiomorpholin-4-yl)-3-methylphenyl]acetic acid Ex.10 methylphenyl]-N- following protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 {[4-methoxy-2-(4- equiv), 12 h at rt, purification by preparative HPLC, yield methylpiperidin- 61%, mp: 101° C., appearance: white solid 1-yl)phenyl](5- 1H NMR (300 MHz, δ in ppm): 0.90 (d, 3H, J = 6.2 Hz), 1.1- methylfuran-2- 1.3 (m, 2H), 1.3-1.4 (m, 1H), 1.4-1.55 (m, 1H), 1.55-1.65 yl)methyl}acetamide (m, 1H), 2.17 (s, 3H), 2.22 (s, 3H), 2.55-2.65 (m, 1H), 2.75- 2.85 (m, 1H), 2.95-3.05 (m, 2H), 3.2-3.3 (m, 8H), 3.36 (s, 2H), 3.71 (s, 3H), 5.80 (d, 1H, J = 2.7 Hz), 5.9-5.95 (m, 1H), 6.39 (d, 1H, J = 8.7 Hz), 6.6-6.7 (m, 2H), 7.0-7.1 (m, 3H), 7.20 (d, 1H, J = 8.3 Hz), 8.68 (d, 1H, J = 8.5 Hz); m/z: 580 [M + H]+ (calc. mass: 579). 14 2-[4-(1,1-dioxo-1- From {4-methoxy-2-[4-(trifluoromethyl)piperidin-1- thiomorpholin-4- yl]phenyl}(5-methylfuran-2-yl)methanamine Ex.14 and 2-[4- yl)-3- (1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid methylphenyl]-N- Ex.10 following protocol A, DMAP (3.2 equiv), EDCl•HCl ({4-methoxy-2-[4- (1.2 equiv), 12 h at rt, purification by preparative HPLC, yield trifluoromethyl) 51%, mp: 106° C., appearance: white solid piperidin-1- 1H NMR (300 MHz, δ in ppm): 1.40-1.65 (m, 4H), 1.75-1.85 yl]phenyl}(5- (m, 1H), 2.17 (s, 3H), 2.22 (s, 3H), 2.45-2.5 (m, 1H), 2.75- methylfuran-2- 2.85 (m, 1H), 2.8-2.9 (m, 1H), 2.95-3.05 (m, 1H), 3.2-3.3 yl)methyl)acetamide (m, 8H), 3.36 (s, 2H), 3.72 (s, 3H), 5.84 (d, 1H, J = 2.8 Hz), 5.9-5.95 (m, 1H), 6.38 (d, 1H, J = 8.5 Hz), 6.65 (d, 1H, J = 2.6 Hz), 6.70 (dd, 1H, J = 8.6 Hz, J = 2.6 Hz), 7.0-7.1 (m, 3H), 7.19 (d, 1H, J = 8.5 Hz), 8.72 (d, 1H, J = 8.5 Hz); m/z: 634 [M + H]+ (calc. mass: 633). 15 N-{[2- From 2-[amino(5-methylfuran-2-yl)methyl]-5-methoxy-N,N- (dimethylamino)- dimethylaniline Ex.15 and 2-[4-(1,1-dioxo-1-thiomorpholin- 4- 4-yl)-3-methylphenyl]acetic acid Ex.10 following protocol A, methoxyphenyl] DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 12 h at rt, (5-methylfuran-2- purification by preparative HPLC, yield 68%, mp: 98° C., yl)methyl}-2-[4- appearance: white solid (1,1-dioxo-1- 1H NMR (300 MHz, δ in ppm): 2.18 (s, 3H), 2.22 (s, 3H), thiomorpholin-4- 2.53 (s, 6H), 3.2-3.28 (m, 8H), 3.37 (s, 2H), 3.73 (s, 3H), yl)-3- 5.73 (d, 1H, J = 2.9 Hz), 5.9-5.93 (m, 1H), 6.40 (d, 1H, methylphenyl] J = 8.3 Hz), 6.65-6.7 (m, 2H), 7.0-7.05 (m, 3H), 7.26 (d, 1H, acetamide J = 9.3 Hz), 8.76 (d, 1H, J = 8.5 Hz); m/z: 526 [M + H]+ (calc. mass: 525). 16 N-[(2-{3- From (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- azabicyclo[3.1.0] methoxyphenyl)(5-methylfuran-2-yl)methanamine Ex.16 hexan-3-yl}-4- and 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3- methoxyphenyl) methylphenyl]acetic acid Ex.10 following protocol A, DMAP (5-methylfuran-2- (3.2 equiv), EDCl•HCl (1.2 equiv), 12 h at rt, purification by yl)methyl]-2-[4- preparative HPLC, yield 42%, mp: 103° C., appearance: (1,1-dioxo-1- white solid thiomorpholin-4- 1H NMR (300 MHz, δ in ppm): 0.30-0.40 (m, 1H), 0.65-0.75 yl)-3- (m, 1H), 1.35-1.45 (m, 2H), 2.19 (s, 3H), 2.23 (s, 3H), 2.93 methylphenyl] (s, 2H), 2.96 (d, 1H, J = 9.3 Hz), 3.12 (d, 1H, J = 8.7 Hz), 3.2- acetamide 3.3 (m, 8H), 3.38 (s, 2H), 3.71 (s, 3H), 5.73 (d, 1H, J = 2.9 Hz), 5.9-5.95 (m, 1H), 6.20 (d, 1H, J = 8.4 Hz), 6.6-6.7 (m, 2H), 7.0-7.1 (m, 3H), 7.19 (d, 1H, J = 9.2 Hz), 8.72 (d, 1H, J = 8.5 Hz); m/z: 564 [M + H]+ (calc. mass: 563). 17 2-[2-(1,1-dioxo-1- From [5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.18 and 2-[2-(1,1-dioxo-1-thiomorpholin- yl)pyrimidin-5-yl]- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, N-{[5-methyl-2- DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, (piperidin-1- purification by column chromatography on silica gel yl)phenyl](5- (CH2Cl2/MeOH, 98:2), yield 75%, mp: 159° C., appearance: methylfuran-2- yellow solid yl)methyl}acetamide 1H NMR (300 MHz, δ in ppm): 1.45-1.52 (m, 6H), 2.18 (s, 3H), 2.23 (s, 3H), 2.51-2.56 (m, 2H), 2.72-2.77 (m, 2H), 3.09-3.12 (m, 4H), 3.37 (s, 2H), 4.16-4.19 (m, 4H), 5.85 (d, 1H, J = 3.0 Hz), 5.94 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.53 (d, 1H, J = 8.4 Hz), 7.04-7.10 (m, 3H), 8.30 (s, 2H), 8.82 (d, 1H, J = 8.4 Hz); m/z: 538 [M + H]+ (calc. mass: 537). 18 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)-2- 4-yl)-2-methylphenyl]acetic acid Ex.19 following protocol A, methylphenyl]-N- substituted amine (1.025 equiv), DMAP (2.2 equiv), {[4-methyl-2- EDCl•HCl (1.2 equiv), 48 h at rt, purification by preparative (piperidin-1- HPLC, yield 41%, mp: 96° C., appearance: white solid yl)phenyl](5- 1H NMR (300 MHz, δ in ppm): 1.35-1.69 (m, 6H), 2.17 (s, methylfuran-2- 3H), 2.18 (s, 3H), 2.25 (s, 3H), 2.52-2.63 (m, 2H), 2.72-2.85 yl)methyl}acetamide (m, 2H), 3.00-3.13 (m, 4H), 3.39 (s, 2H), 3.62-3.79 (m, 4H), 5.81 (d, 1H, J = 3.0 Hz), 5.93 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.49 (d, 1H, J = 8.5 Hz), 6.74 (dd, 1H, J = 8.4 Hz, J = 2.6 Hz), 6.80 (d, 1H, J = 2.5 Hz), 6.89 (d, 1H, J = 7.9 Hz), 6.94 (s, 1H), 7.04 (d, 1H, J = 8.3 Hz), 7.19 (d, 1H, J = 7.8 Hz), 8.62 (d, 1H, J = 8.5 Hz); m/z: 550 [M + H]+ (calc. mass: 549). 19 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2- (5-methylfuran-2- methylphenyl]acetic acid Ex.19 following protocol A, yl)methyl]-2-[4- substituted amine (0.9 equiv), DMAP (2.2 equiv), EDCl•HCl (1,1-dioxo-1- (1.2 equiv), 48 h at rt, purification by preparative HPLC, yield thiomorpholin-4- 21%, mp: 178° C., appearance: white solid yl)-2- 1H NMR (300 MHz, δ in ppm): 2.19 (s, 6H), 2.20 (s, 3H), methylphenyl] 2.24 (s, 3H), 2.99-3.14 (m, 4H), 3.41 (s, 2H), 3.62-3.77 (m, acetamide 4H), 5.85 (d, 1H, J = 2.5 Hz), 5.97 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.12 (d, 1H, J = 8.3 Hz), 6.75 (dd, 1H, J = 8.1 Hz, J = 2.7 Hz), 6.80 (d, 1H, J = 2.3 Hz), 6.94-7.02 (m, 2H), 7.05 (d, 1H, J = 8.4 Hz), 7.11 (d, 1H, J = 8.4 Hz), 8.85 (d, 1H, J = 8.2 Hz); m/z: 503 [M + Na]+ (calc. mass: 480). 20 2-[2-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[2-(1,1-dioxo-1-thiomorpholin- yl)pyrimidin-5-yl]- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, N-{[4-methyl-2- DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, (piperidin-1- purification by preparative HPLC, yield 26%, mp: 91° C., yl)phenyl](5- appearance: pale yellow solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 1.46-1.53 (m, 6H), 2.18 (s, yl)methyl}acetamide 3H), 2.25 (s, 3H), 2.52-2.60 (m, 2H), 2.76-2.80 (m, 2H), 3.08-3.12 (m, 4H), 3.36 (s, 2H), 4.16-4.19 (m, 4H), 5.83 (d, 1H, J = 3.0 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.49 (d, 1H, J = 8.4 Hz), 6.90 (d, 1H, J = 8.0 Hz), 6.95 (s, 1H), 7.19 (d, 1H, J = 7.8 Hz), 8.29 (s, 2H), 8.81 (d, 1H, J = 8.4 Hz); m/z: 538 [M + H]+ (calc. mass: 537). 21 N-[(2-bromo-4- From (2-bromo-4-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.12 and 2-[4-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)-2-methylphenyl]acetic acid Ex.19 following protocol A, yl)methyl]-2-[4- substituted amine (1.025 equiv), DMAP (3.2 equiv), (1,1-dioxo-1- EDCl•HCl (1.2 equiv), 48 h at rt, purification by preparative thiomorpholin-4- HPLC, yield 20%, mp: 173° C., appearance: white solid yl)-2- 1H NMR (300 MHz, δ in ppm): 2.19 (s, 3H), 2.21 (s, 3H), methylphenyl] 2.28 (s, 3H), 3.00-3.15 (m, 4H), 3.43 (s, 2H), 3.63-3.77 (m, acetamide 4H), 5.77 (d, 1H, J = 3.3 Hz), 5.97 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 6.27 (d, 1H, J = 8.2 Hz), 6.75 (dd, 1H, J = 8.2 Hz, J = 2.6 Hz), 6.80 (d, 1H, J = 2.5 Hz), 7.03 (d, 1H, J = 8.3 Hz), 7.20 (d, 1H, J = 9.0 Hz), 7.33 (d, 1H, J = 8.0 Hz), 7.43 (s, 1H), 8.99 (d, 1H, J = 8.3 Hz); m/z: 567 [M + Na]+, 569 [M + Na]+ (calc. mass: 544). 22 N-[(2-{3- From (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- azabicyclo[3.1.0] methylphenyl)(phenyl)methanamine Ex.21 and 2-[4-(1,1- hexan-3-yl}-4- dioxo-1-thiomorpholin-4-yl)phenyl]acetic acid Ex.1 following methylphenyl) protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 48 h at (phenyl) rt, purification by column chromatography on silica gel methyl]-2-[4- (CH2Cl2/MeOH, 98:2), yield 45%, mp: 104° C., appearance: (1,1-dioxo-1- white solid thiomorpholin-4- 1H NMR (300 MHz, δ in ppm): 0.29-0.36 (m, 1H), 0.61-0.65 yl)phenyl]acetamide (m, 1H), 1.39-1.42 (m, 2H), 2.23 (s, 3H), 2.77-2.84 (m, 2H), 3.04-3.11 (m, 5H), 3.20 (d, 1H, J = 8.7 Hz), 3.41 (s, 2H), 3.71- 3.74 (m, 4H), 6.37 (d, 1H, J = 8.6 Hz), 6.83 (d, 1H, J = 6.9 Hz), 6.93-6.97 (m, 3H), 7.03-7.07 (m, 3H), 7.13-7.19 (m, 3H), 7.23-7.28 (m, 2H), 8.66 (d, 1H, J = 8.6 Hz); m/z: 530 [M + H]+ (calc. mass: 529). 23 N-[(2-{3- From (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4- azabicyclo[3.1.0] methylphenyl)(phenyl)methanamine Ex.21 and 2-[4-(1,1- hexan-3-yl}-4- dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetic acid methylphenyl) Ex.10 following protocol A, DMAP (3.2 equiv), EDCl•HCl (phenyl) (1.2 equiv), 48 h at rt, purification by column methyl]-2-[4- chromatography on silica gel (CH2Cl2/MeOH, 98:2) (1,1-dioxo-1- followed by recristallisation using a mixture of Et2O and thiomorpholin-4- cyclohexane, yield 19%, mp: 109° C., appearance: white yl)-3- solid methylphenyl] 1H NMR (300 MHz, δ in ppm): 0.29-0.36 (m, 1H), 0.61-0.65 acetamide (m, 1H), 1.39-1.42 (m, 2H), 2.23 (s, 6H), 2.77-2.85 (m, 2H), 3.05 (d, 1H, J = 8.4 Hz), 3.18 (d, 1H, J = 8.7 Hz), 3.24-3.26 (m, 8H), 3.42 (s, 2H), 6.37 (d, 1H, J = 8.6 Hz), 6.84 (d, 1H, J = 7.9 Hz), 6.98 (s, 1H), 7.03-7.7 (m, 3H), 7.06-7.08 (m, 3H), 7.15-7.20 (m, 1H), 7.23-7.28 (m, 2H), 8.70 (d, 1H, J = 8.6 Hz); m/z: 544 [M + H]+ (calc. mass: 543). 24 2-[4-(1,1-dioxo-1- From [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.11 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-{[4- 4-yl)phenyl]acetic acid Ex.1 following protocol A, DMAP methyl-2- (2.2 equiv), EDCl•HCl (1.2 equiv), 48 h at rt, purification by (trifluoromethyl) column chromatography on silica gel (CH2Cl2/MeOH, phenyl](5- 98:2), yield 38%, mp: 90° C., appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 2.19 (s, 3H), 2.36 (s, 3H), yl)methyl}acetamide 3.07-3.10 (m, 4H), 3.38 (s, 2H), 3.70-3.73 (m, 4H), 5.74 (d, 1H, J = 3.1 Hz), 5.95 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 6.31 (d, 1H, J = 7.8 Hz), 6.93 (d, 2H, J = 8.8 Hz), 7.11 (d, 2H, J = 8.7 Hz), 7.49-7.56 (m, 3H), 9.02 (d, 1H, J = 8.0 Hz); m/z: 543 [M + Na]+ (calc. mass: 520). 25 N-{[4-methyl-2- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- (piperidin-1- yl)methanamine Ex.6 and 2-[6-(morpholin-4-yl)pyridin-3- yl)phenyl](5- yl]acetic acid Ex.22 following protocol A, DMAP (2.2 equiv), methylfuran-2- EDCl•HCl (1.2 equiv), 48 h at rt, purification by column yl)methyl}-2-[6- chromatography on silica gel (CH2Cl2/MeOH, 98:2), yield (morpholin-4- 33%, mp: 61° C., appearance: pale brown solid yl)pyridin-3- 1H NMR (300 MHz, δ in ppm): 1.46-1.54 (m, 6H), 2.17 (s, yl]acetamide 3H), 2.25 (s, 3H), 2.54-2.59 (m, 2H), 2.76-2.80 (m, 2H), 3.31 (s, 2H), 3.36 (t, 4H, J = 5.1 Hz), 3.67 (t, 4H, J = 5.1 Hz), 5.81 (d, 1H, J = 2.9 Hz), 5.92 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.47 (d, 1H, J = 8.4 Hz), 6.76 (d, 1H, J = 8.7 Hz), 6.89 (d, 1H, J = 8.0 Hz), 6.94 (s, 1H), 7.17 (d, 1H, J = 7.8 Hz), 7.43 (dd, 1H, J = 8.7 Hz, J = 2.4 Hz), 7.97 (d, 1H, J = 2.0 Hz), 8.71 (s, 1H, J = 8.4 Hz); m/z: 489 [M + H]+ (calc. mass: 488). 26 N-{[4-methyl-2- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- (piperidin-1- yl)methanamine Ex.6 and 2-[2-(morpholin-4-yl)pyrimidin-5- yl)phenyl](5- yl]acetic acid Ex.23 following protocol A, DMAP (2.2 equiv), methylfuran-2- EDCl•HCl (1.2 equiv), 48 h at rt, purification by column yl)methyl}-2-[2- chromatography on silica gel (Cyclohexane/EtOAc, 60:40), (morpholin-4- yield 67%, mp: 69° C., appearance: pale yellow solid yl)pyrimidin-5- 1H NMR (300 MHz, δ in ppm): 1.46-1.53 (m, 6H), 2.17 (s, yl]acetamide 3H), 2.25 (s, 3H), 2.54-2.60 (m, 2H), 2.72-2.80 (m, 2H), 3.31 (s, 2H), 3.63 (s, 8H), 5.83 (d, 1H, J = 2.7 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.48 (d, 1H, J = 8.3 Hz), 6.90 (d, 1H, J = 7.9 Hz), 6.95 (s, 1H), 7.18 (d, 1H, J = 7.8 Hz), 8.22 (s, 2H), 8.77 (d, 1H, J = 8.4 Hz); m/z: 490 [M + H]+ (calc. mass: 489). 27 2-[6-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[6-(1,1-dioxo-1-thiomorpholin- yl)pyridin-3-yl]-N- 4-yl)pyridin-3-yl]acetic acid Ex.24 following protocol A, {[4-methyl-2- DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), 16 h at rt, (piperidin-1- purification by column chromatography on silica gel yl)phenyl](5- (Cyclohexane/EtOAc, 50:50), yield 55%, mp: 102° C., methylfuran-2- appearance: white solid yl)methyl} 1H NMR (300 MHz, δ in ppm): 1.45-1.54 (m, 6H), 2.17 (s, acetamide 3H), 2.25 (s, 3H), 2.52-2.58 (m, 2H), 2.73-2.79 (m, 2H), 3.02-3.06 (m, 4H), 3.53 (s, 2H), 3.99-4.01 (m, 4H), 5.82 (d, 1H, J = 2.7 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.47 (d, 1H, J = 8.4 Hz), 6.89 (d, 1H, J = 7.9 Hz), 6.94-6.97 (m, 2H), 7.16 (d, 1H, J = 7.8 Hz), 7.48 (dd, 1H, J = 8.7 Hz, J = 2.4 Hz), 8.00 (d, 1H, J = 2.1 Hz), 8.73 (d, 1H, J = 8.4 Hz); m/z: 537 [M + H]+ (calc. mass: 536). 28 N-[(2-{3- From (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5- azabicyclo[3.1.0] methylfuran-2-yl)methanamine Ex.25 and 2-[5-(1,1-dioxo-1- hexan-3-yl}-4- thiomorpholin-4-yl)-2-methylphenyl]acetic acid Ex.3 methylphenyl)(5- following protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 methylfuran-2- equiv), 16 h at rt, purification by column chromatography on yl)methyl]-2-[5- silica gel (Cyclohexane/EtOAc, 60:40), yield 49%, mp: (1,1-dioxo-1- 94° C., appearance: white solid thiomorpholin-4- 1H NMR (300 MHz, δ in ppm): 0.33-0.39 (m, 1H), 0.71-0.75 yl)-2- (m, 1H), 1.41-1.44 (m, 2H), 2.13 (s, 3H), 2.19 (s, 3H), 2.24 methylphenyl] (s, 3H), 2.89-2.91 (m, 2H), 2.98 (dd, 1H, J = 8.4 Hz, J = 2.6 Hz), acetamide 3.05-3.08 (m, 4H), 3.11 (d, 1H, J = 8.6 Hz), 3.42-3.43 (m, 2H), 3.63-3.67 (m, 4H), 5.72 (d, 1H, J = 2.9 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.29 (d, 1H, J = 8.6 Hz), 6.77 (dd, 1H, J = 8.3 Hz, J = 2.7 Hz), 6.85-6.88 (m, 2H), 6.93 (s, 1H), 6.98 (d, 1H, J = 8.5 Hz), 7.21 (d, 1H, J = 7.8 Hz), 8.72 (d, 1H, J = 8.7 Hz); m/z: 548 [M + H]+ (calc. mass: 547). 29 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)-3- 4-yl)-3-methoxyphenyl]acetic acid Ex.26 following protocol methoxyphenyl]- A, substituted amine (0.09 equiv), DMAP (2.2 equiv), N-{[4-methyl-2- EDCl•HCl (1.2 equiv), 12 h at rt, purification by preparative (piperidin-1- HPLC, yield 40%, mp: 90° C., appearance: white solid yl)phenyl](5- 1H NMR (300 MHz, δ in ppm): 1.38-1.62 (m, 6H), 2.17 (s, methylfuran-2- 3H), 2.25 (s, 3H), 2.53-2.59 (m, 2H), 2.71-2.81 (m, 2H), yl)methyl}acetamide 3.14-3.23 (m, 4H), 3.33-3.40 (m, 6H), 3.73 (s, 3H), 5.80 (d, 1H, J = 2.9 Hz), 5.92 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.48 (d, 1H, J = 8.5 Hz), 6.74 (dd, 1H, J = 8.1 Hz, J = 1.7 Hz), 6.85-6.95 (m, 4H), 7.20 (d, 1H, J = 7.8 Hz), 8.72 (d, 1H, J = 8.5 Hz); -m/z: 566 [M + H]+ (calc. mass: 565). 30 2-[3-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[3-(1,1-dioxo-1-thiomorpholin- yl)-4- 4-yl)-4-methoxyphenyl]acetic acid Ex.27 following protocol methoxyphenyl]- A, substituted amine (0.09 equiv), DMAP (2.2 equiv), N-{[4-methyl-2- EDCl•HCl (1.2 equiv), 12 h at rt, purification by preparative (piperidin-1- HPLC, yield 47%, mp: 88° C., appearance: white solid yl)phenyl](5- 1H NMR (300 MHz, δ in ppm): 1.40-1.60 (m, 6H), 2.17 (s, methylfuran-2- 3H), 2.25 (s, 3H), 2.52-2.59 (m, 2H), 2.71-2.81 (m, 2H), yl)methyl}acetamide 3.16-3.25 (m, 4H), 3.32-3.40 (m, 6H), 3.75 (s, 3H), 5.80 (d, 1H, J = 2.9 Hz), 5.92 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.48 (d, 1H, J = 8.8 Hz), 6.83-6.95 (m, 5H), 7.20 (d, 1H, J = 7.8 Hz), 8.69 (d, 1H, J = 8.6 Hz); m/z: 566 [M + H]+ (calc. mass: 565). 31 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- (5-methylfuran-2- yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following yl)methyl]-1-[4- protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at (1,1-dioxo-1- rt, purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 60:40), yield 80%, mp: 75° C., yl)phenyl] appearance: white solid cyclopropane-1- 1H NMR (300 MHz, δ in ppm): 0.92-0.97 (m, 2H), 1.23-1.33 carboxamide (m, 2H), 2.15 (s, 3H), 2.16 (s, 3H), 2.22 (s, 3H), 3.07-3.10 (m, 4H), 3.75-3.78 (m, 4H), 5.78 (d, 1H, J = 3.1 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.08 (d, 1H, J = 8.3 Hz), 6.88 (d, 1H, J = 7.9 Hz), 6.92-6.95 (m, 2H), 6.99-7.05 (m, 3H), 7.23-7.26 (m, 2H); m/z: 493 [M + H]+ (calc. mass: 492). 32 1-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 1-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-{[4- 4-yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following methyl-2- protocol A, DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 16 h at (piperidin-1- rt, purification by column chromatography on silica gel yl)phenyl](5- (Cyclohexane/EtOAc, 60:40), yield 78%, mp: 98° C., methylfuran-2- appearance: white solid yl)methyl} 1H NMR (300 MHz, δ in ppm): 0.92-0.94 (m, 2H), 1.23-1.39 cyclopropane-1- (m, 8H), 2.11 (s, 3H), 2.23 (s, 3H), 2.42-2.45 (m, 2H), 2.57- carboxamide 2.63 (m, 2H), 3.08-3.10 (m, 4H), 3.74-3.76 (m, 4H), 5.81 (dd, 1H, J = 2.9 Hz, J = 0.7 Hz), 5.92 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.32 (d, 1H, J = 8.8 Hz), 6.86 (d, 1H, J = 8.0 Hz), 6.97-7.02 (m, 5H), 7.24-7.27 (m, 2H); m/z: 562 [M + H]+ (calc. mass: 561). 33 2-[2-(1,1-dioxo-1- From [4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.11 and 2-[2-(1,1-dioxo-1-thiomorpholin- yl)pyrimidin-5-yl]- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, N-{[4-methyl-2- substituted amine (0.09 equiv), DMAP (2.2 equiv), (trifluoromethyl) EDCl•HCl (1.2 equiv), 48 h at rt, purification by preparative phenyl](5- HPLC, yield 41%, mp: 224° C., appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 2.19 (s, 3H), 2.37 (s, 3H), yl)methyl}acetamide 3.11 (t, 4H, J = 5.5 Hz), 3.36-3.41 (m, 2H), 4.18 (t, 4H, J = 5.3 Hz), 5.79 (d, 1H, J = 2.7 Hz), 5.96 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.30 (d, 1H, J = 7.9 Hz), 7.49-7.59 (m, 3H), 8.28 (s, 2H), 9.14 (d, 1H, J = 8.1 Hz); m/z: 523 [M + H]+ (calc. mass: 522). 34 N-[(2-bromo-4- From (2-bromo-4-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.12 and 2-[2-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, yl)methyl]-2-[2- substituted amine (0.09 equiv), DMAP (3.2 equiv), (1,1-dioxo-1- EDCl•HCl (1.2 equiv), 48 h at rt, purification by preparative thiomorpholin-4- HPLC, yield 21%, mp: 199° C., appearance: white solid yl)pyrimidin-5- 1H NMR (300 MHz, δ in ppm): 2.21 (s, 3H), 2.28 (s, 3H), yl]acetamide 3.10 (t, 4H, J = 4.1 Hz), 3.40 (s, 2H), 4.18 (t, 4H, J = 5.0 Hz), 5.81 (d, 1H, J = 2.6 Hz), 5.97 (dd, 1H, J = 3 Hz, J = 1.1 Hz), 6.24 (d, 1H, J = 8.2 Hz), 7.21 (d, 1H, J = 9.5 Hz), 7.31 (d, 1H, J = 7.9 Hz), 7.43 (s, 1H), 8.30 (s, 2H), 9.13 (d, 1H, J = 8.0 Hz); m/z: 555 [M + Na]+, 557 [M + Na]+ (calc. mass: 532). 35 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5- (5-methylfuran-2- yl]acetic acid Ex.17 following protocol A, substituted amine yl)methyl]-2-[2- (0.09 equiv), DMAP (3.2 equiv), EDCl•HCl (1.2 equiv), 48 h (1,1-dioxo-1- at rt, purification by preparative HPLC, yield 32%, mp: thiomorpholin-4- 208° C., appearance: white solid yl)pyrimidin-5- 1H NMR (300 MHz, δ in ppm): 2.18 (s, 3H), 2.20 (s, 3H), yl]acetamide 2.23 (s, 3H), 3.11 (t, 4H, J = 4.9 Hz), 3.39 (s, 2H), 4.11-4.23 (m, 4H), 5.87 (d, 1H, J = 3.1 Hz), 5.95-6.00 (m, 1H), 6.10 (d, 1H, J = 8.0 Hz), 6.94-7.02 (m, 2H), 7.10 (d, 1H, J = 7.8 Hz), 8.30 (s, 2H), 9.00 (d, 1H, J = 8.3 Hz); m/z: 491 [M + Na]+ (calc. mass: 468). 36 N-[(2-{3- From (2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5- azabicyclo[3.1.0] methylfuran-2-yl)methanamine Ex.25 and 2-[2-(1,1-dioxo-1- hexan-3-yl}-4- thiomorpholin-4-yl)pyrimidin-5-yl]acetic acid Ex.17 following methylphenyl)(5- protocol A, substituted amine (0.09 equiv), DMAP (2.2 methylfuran-2- equiv), EDCl•HCl (1.2 equiv), 48 h at rt, purification by yl)methyl]-2-[2- column chromatography on silica gel (Cyclohexane/EtOAc, (1,1-dioxo-1- 40:60), yield 35%, mp: 105° C., appearance: white solid thiomorpholin-4- 1H NMR (300 MHz, δ in ppm): 0.31-0.40 (m, 1H), 0.70-0.76 yl)pyrimidin-5- (m, 1H), 1.40-1.45 (m, 2H), 2.19 (s, 3H), 2.24 (s, 3H), 2.90 yl]acetamide (s, 2H), 3.08-3.13 (m, 4H), 3.28-3.31 (m, 2H), 3.33-3.37 (m, 2H), 4.12-4.22 (m, 4H), 5.75 (d, 1H, J = 3.3 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.27 (d, 1H, J = 8.3 Hz), 6.86 (d, 1H, J = 7.3 Hz), 6.94 (s, 1H), 7.18 (d, 1H, J = 7.8 Hz), 8.29 (s, 2H), 8.84 (d, 1H, J = 8.5 Hz); m/z: 536 [M + H]+ (calc. mass: 535). 37 1-[3-bromo-4-(1,1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- dioxo-1- yl)methanamine Ex.6 and 1-[3-bromo-4-(1,1-dioxo-1- thiomorpholin-4- thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid yl)phenyl]-N-{[4- Ex.29 following protocol A, substituted amine (0.09 equiv), methyl-2- DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), 14 h at rt, (piperidin-1- purification by column chromatography on silica gel yl)phenyl](5- (Cyclohexane/EtOAc, 40:60), yield 71%, mp: 106° C., methylfuran-2- appearance: white solid yl)methyl} 1H NMR (300 MHz, δ in ppm): 0.92-1.06 (m, 2H), 1.18-1.47 cyclopropane-1- (m, 8H), 2.14 (s, 3H), 2.24 (s, 3H), 2.39-2.46 (m, 2H), 2.57- carboxamide 2.66 (m, 2H), 3.23-3.31 (m, 4H), 3.34-3.42 (m, 4H), 5.79 (d, 1H, J = 2.3 Hz), 5.92 (dd, 1H, J = 3.1 Hz, J = 1.1 Hz), 6.38 (d, 1H, J = 8.8 Hz), 6.88 (dd, 1H, J = 7.6 Hz, J = 1.1 Hz), 6.98 (s, 1H), 7.10 (d, 1H, J = 7.7 Hz), 7.24 (d, 1H, J = 8.3 Hz), 7.32 (dd, 1H, J = 8.2 Hz, J = 2.0 Hz), 7.58 (d, 1H, J = 2.0 Hz), 7.68 (d, 1H, J = 8.8 Hz); m/z: 640 [M + H]+, 642 [M + H]+ (calc. mass: 639). 38 2-[2-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[2-(1,1-dioxo-1-thiomorpholin- yl)-4- 4-yl)-4-methylpyrimidin-5-yl]acetic acid Ex.30 following methylpyrimidin- protocol A, substituted amine (0.09 equiv), DMAP (2.2 5-yl]-N-{[4- equiv), EDCl•HCl (1.2 equiv), 24 h at rt, purification by methyl-2- column chromatography on silica gel (Cyclohexane/EtOAc, (piperidin-1- 50:50), yield 15%, mp: 99° C., appearance: white solid yl)phenyl](5- 1H NMR (300 MHz, δ in ppm): 1.41-1.60 (m, 6H), 2.18 (s, methylfuran-2- 3H), 2.26 (s, 6H), 2.57-2.65 (m, 2H), 2.75-2.82 (m, 2H), yl)methyl}acetamide 3.05-3.13 (m, 4H), 3.41 (s, 2H), 4.13-4.22 (m, 4H), 5.83 (d, 1H, J = 2.6 Hz), 5.94 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.51 (d, 1H, J = 8.7 Hz), 6.91 (d, 1H, J = 7.7 Hz), 6.95 (s, 1H), 7.21 (d, 1H, J = 7.7 Hz), 8.11 (s, 1H), 8.79 (d, 1H, J = 8.4 Hz); m/z: 552 [M + H]+ (calc. mass: 551). 39 2-[3-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[3-(1,1-dioxo-1-thiomorpholin- yl)-4- 4-yl)-4-hydroxyphenyl]acetic acid Ex.31 following protocol hydroxyphenyl]- A, substituted amine (0.09 equiv), DMAP (2.2 equiv), N-{[4-methyl-2- EDCl•HCl (1.2 equiv), 24 h at rt, purification by column (piperidin-1- chromatography on silica gel (Cyclohexane/EtOAc, 50:50), yl)phenyl](5- yield 36%, mp: 118° C., appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 1.39-1.58 (m, 6H), 2.17 (s, yl)methyl}acetamide 3H), 2.25 (s, 3H), 2.54-2.60 (m, 2H), 2.73-2.80 (m, 2H), 3.21-3.29 (m, 10H), 5.79 (d, 1H, J = 2.7 Hz), 5.92 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.47 (d, 1H, J = 8.5 Hz), 6.69 (d, 1H, J = 8.2 Hz), 6.76 (dd, 1H, J = 7.6 Hz, J = 1.7 Hz), 6.90 (d, 1H, J = 8.5 Hz), 6.93 (s, 2H), 7.19 (d, 1H, J = 7.7 Hz), 8.66 (d, 1H, J = 9.0 Hz), 8.87 (s, 1H); m/z: 552 [M + H]+ (calc. mass: 551). 40 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2- (5-methylfuran-2- methylpropanoic acid Ex.32 following protocol A, yl)methyl]-2-[4- substituted amine (0.09 equiv), DMAP (3.2 equiv), (1,1-dioxo-1- EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the reaction thiomorpholin-4- mixture to dryness and purification by column yl)phenyl]-2- chromatography on silica gel (Cyclohexane/EtOAc, 60:40), methylpropanamide yield 55%, mp: 67° C., appearance: white solid 1H NMR (300 MHz, δ in ppm): 1.43 (s, 6H), 2.15 (s, 3H), 2.17 (s, 3H), 2.22 (s, 3H), 3.06-3-12 (m, 4H), 3.70-3.76 (m, 4H), 5.68 (d, 1H, J = 3.0 Hz), 5.91 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.16 (d, 1H, J = 8.7 Hz), 6.89-6.94 (m, 3H), 6.96 (d, 2H, J = 9.1 Hz), 7.18 (d, 2H, J = 8.9 Hz), 7.88 (d, 1H, J = 8.3 Hz); m/z: 517 [M + Na]+ (calc. mass: 494). 41 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- (5-methylfuran-2- yl)phenyl]cyclobutane-1-carboxylic acid Ex.33 following yl)methyl]-1-[4- protocol A, substituted amine (0.09 equiv), DMAP (3.2 (1,1-dioxo-1- equiv), EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the thiomorpholin-4- reaction mixture to dryness and purification by column yl)phenyl] chromatography on silica gel (Cyclohexane/EtOAc, 60:40), cyclobutane-1- yield 33%, mp: 79° C., appearance: white solid carboxamide 1H NMR (300 MHz, δ in ppm): 1.70-1.74 (m, 2H), 2.06 (s, 3H), 2.16 (s, 3H), 2.20 (s, 3H), 2.30-2.40 (m, 2H), 2.60-2.70 (m, 2H), 3.06-3.12 (m, 4H), 3.63-3.70 (m, 4H), 5.63 (d, 1H, J = 3.2 Hz), 5.90 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.07 (d, 1H, J = 8.1 Hz), 6.85 (s, 2H), 6.92 (s, 1H), 6.97 (d, 2H, J = 8.9 Hz), 7.26 (d, 2H, J = 8.8 Hz), 8.21 (d, 1H, J = 8.5 Hz); m/z: 529 [M + Na]+ (calc. mass: 506). 42 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (5-methylfuran-2- methylpyrimidin-5-yl]acetic acid Ex.30 following protocol A, yl)methyl]-2-[2- substituted amine (0.09 equiv), DMAP (3.2 equiv), (1,1-dioxo-1- EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the reaction thiomorpholin-4- mixture to dryness and purification by column yl)-4- chromatography on silica gel (Cyclohexane/EtOAc, 50:50), methylpyrimidin- yield 22%, mp: 211° C., appearance: white solid 5-yl]acetamide 1H NMR (300 MHz, δ in ppm): 2.19 (s, 3H), 2.21 (s, 3H), 2.24 (s, 3H), 2.26 (s, 3H), 3.06-3.12 (m, 4H), 3.44 (s, 2H), 4.15-4.21 (m, 4H), 5.87 (d, 1H, J = 2.7 Hz), 5.98 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.11 (d, 1H, J = 8.0 Hz), 6.98-7.01 (m, 2H), 7.12 (d, 1H, J = 7.5 Hz), 8.13 (s, 1H), 9.00 (d, 1H, J = 8.6 Hz); m/z: 483 [M + H]+ (calc. mass: 482). 43 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- 5-methylfuran-2- hydroxyphenyl]acetic acid Ex.31 following protocol A, yl)methyl]-2-[3- substituted amine (0.09 equiv), DMAP (3.2 equiv), (1,1-dioxo-1- EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the reaction thiomorpholin-4- mixture to dryness and purification by column yl)-4- chromatography on silica gel (Cyclohexane/EtOAc, 40:60), hydroxyphenyl] yield 17%, mp: 146° C., appearance: white solid acetamide 1H NMR (300 MHz, δ in ppm): 2.16 (s, 3H), 2.20 (s, 3H), 2.23 (s, 3H), 3.22-3.29 (m, 8H), 3.30 (s, 2H), 5.83 (d, 1H, J = 3.2 Hz), 5.96 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.09 (d, 1H, J = 8.3 Hz), 6.69 (d, 1H, J = 8.2 Hz), 6.76 (dd, 1H, J = 8.0 Hz, J = 1.8 Hz), 6.93-6.96 (m, 2H), 6.98 (d, 1H, J = 8.2 Hz), 7.10 (d, 1H, J = 7.8 Hz), 8.86-8.89 (m, 2H); m/z: 505 [M + Na]+ (calc. mass: 482). 44 1-[4-(1,1-dioxo-1- From (4-methoxy-2-methylphenyl)(5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.34 and 1-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-[(4- 4-yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following methoxy-2- protocol A, substituted amine (0.09 equiv), DMAP (3.2 methylphenyl)(5- equiv), EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the methylfuran-2- reaction mixture to dryness and purification by column yl)methyl] chromatography on silica gel (Cyclohexane/EtOAc, 40:60), cyclopropane-1- yield 35%, mp: 77° C., appearance: white solid carboxamide 1H NMR (300 MHz, δ in ppm): 0.90-1.00 (m, 2H), 1.20-1.33 (m, 2H), 2.16 (s, 6H), 3.05-3.11 (m, 4H), 3.70 (s, 3H), 3.74- 3.79 (m, 4H), 5.78 (d, 1H, J = 2.6 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.07 (d, 1H, J = 8.3 Hz), 6.67-6.72 (m, 2H), 6.90 (d, 1H, J = 8.4 Hz), 6.98-7.04 (m, 3H), 7.24 (d, 2H, J = 8.8 Hz); m/z: 531 [M + Na]+ (calc. mass: 508). 45 N-{[2-(azepan-1- From [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2- yl)-4- yl)methanamine Ex.35 and 2-[2-(1,1-dioxo-1-thiomorpholin- methoxyphenyl] 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, (5-methylfuran-2- substituted amine (0.09 equiv), DMAP (4.2 equiv), yl)methyl}-2-[2- EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the reaction (1,1-dioxo-1- mixture to dryness and purification by column thiomorpholin-4- chromatography on silica gel (Cyclohexane/EtOAc, 40:60), yl)pyrimidin-5- yield 24%, mp: 106° C., appearance: white solid yl]acetamide 1H NMR (300 MHz, δ in ppm): 1.44-1.70 (m, 8H), 2.18 (s, 3H), 2.80-2.88 (m, 2H), 2.92-3.00 (m, 2H), 3.07-3.13 (m, 4H), 3.35 (s, 2H), 3.71 (s, 3H), 4.15-4.19 (m, 4H), 5.75 (d, 1H, J = 2.9 Hz), 5.93 (dd, 1H, J = 2.9 Hz, J = 1.1 Hz), 6.54 (d, 1H, J = 8.8 Hz), 6.65-6.71 (m, 2H), 7.22 (d, 1H, J = 9.3 Hz), 8.29 (s, 2H), 8.80 (d, 1H, J = 8.5 Hz); m/z: 568 [M + H]+ (calc. mass: 567). 46 N-{[2-(azepan-1- From [2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2- yl)-4- yl)methanamine Ex.35 and 1-[4-(1,1-dioxo-1-thiomorpholin- methoxyphenyl] 4-yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following (5-methylfuran-2- protocol A, substituted amine (0.09 equiv), DMAP (3.2 yl)methyl}-1-[4- equiv), EDCl•HCl (1.2 equiv), 18 h at rt. Evaporation of the (1,1-dioxo-1- reaction mixture to dryness and purification by column thiomorpholin-4- chromatography on silica gel (Cyclohexane/EtOAc, 40:60), yl)phenyl] yield 18%, mp: 90° C., appearance: white solid cyclopropane-1- 1H NMR (300 MHz, δ in ppm): 0.89-0.96 (m, 2H), 1.22-1.33 carboxamide (m, 2H), 1.4-1.67 (m, 8H), 2.14 (s, 3H), 2.71-2.81 (m, 2H), 2.86-2.91 (m, 2H), 3.06-3.10 (m, 4H), 3.70 (s, 3H), 3.74- 3.78 (m, 4H), 5.72 (d, 1H, J = 2.5 Hz), 5.90 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.43 (d, 1H, J = 8.3 Hz), 6.61 (dd, 1H, J = 8.5 Hz, J = 2.6 Hz), 6.68 (d, 1H, J = 2.6 Hz), 6.84 (d, 1H, J = 8.9 Hz), 6.96 (d, 1H, J = 8.6 Hz), 7.00 (d, 2H, J = 8.8 Hz), 7.24 (d, 2H, J = 8.7 Hz); m/z: 592 [M + H]+ (calc. mass: 591). 47 2-[5-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[5-(1,1-dioxo-1-thiomorpholin- yl)pyridin-2-yl]-N- 4-yl)pyridin-2-yl]acetic acid Ex.36 following protocol A, {[4-methyl-2- DMAP (1 equiv), EDCl•HCl (1.1 equiv), 2 h at rt, purification (piperidin-1- by column chromatography on silica gel (CH2Cl2/MeOH, yl)phenyl](5- 95:5), yield 54%, mp: 102° C., appearance: white solid methylfuran-2- 1H NMR (300 MHz, δ in ppm): 1.40-1.60 (m, 6H), 2.17 (s, yl)methyl}acetamide 3H), 2.25 (s, 3H), 2.50-2.60 (m, 2H), 2.75-2.85 (m, 2H), 3.10-3.14 (m, 4H), 3.56 (s, 2H), 3.75-3.79 (m, 4H), 5.85 (d, 1H, J = 2.8 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.49 (d, 1H, J = 8.5 Hz), 6.90 (d, 1H, J = 7.8 Hz), 6.94 (s, 1H), 7.17 (d, 1H, J = 8.6 Hz), 7.20 (d, 1H, J = 7.8 Hz), 7.38 (dd, 1H, J = 8.6 Hz, J = 3.1 Hz), 8.23 (d, 1H, J = 2.8 Hz), 8.75 (d, 1H, J = 8.5 Hz); m/z: 537 [M + H]+ (calc. mass: 536). 48 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5- (5-methylfuran-2- yl]cyclopropane-1-carboxylic acid Ex.37 following protocol yl)methyl]-1-[2- A, DMAP (2 equiv), EDCl•HCl (1.1 equiv), 2 h at rt. Sat. (1,1-dioxo-1- NH4Cl was added and the precipitate was collected by thiomorpholin-4- filtration. The title compound was pure as such, yield 75%, yl)pyrimidin-5- mp: 82° C., appearance: white solid yl]cyclopropane- 1H NMR (300 MHz, δ in ppm): 0.92-1.05 (m, 2H), 1.29-1.40 1-carboxamide (m, 2H), 2.16 (s, 3H), 2.18 (s, 3H), 2.23 (s, 3H), 3.09-3.15 (m, 4H), 4.17-4.23 (m, 4H), 5.70 (d, 1H, J = 2.6 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.18 (d, 1H, J = 8.2 Hz), 6.90-6.97 (m, 2H), 7.03 (d, 1H, J = 8.4 Hz), 8.11 (d, 1H, J = 8.3 Hz), 8.35 (s, 2H); m/z: 495 [M + H]+ (calc. mass: 494). 49 N-[(4-chloro-2- From (4-chloro-2-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.38 and 2-[2-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, yl)methyl]-2-[2- DMAP (1.2 equiv), EDCl•HCl (1.1 equiv), overnight at rt. (1,1-dioxo-1- Sat. NH4Cl was added and the precipitate was collected by thiomorpholin-4- filtration and washed with water. The title compound was yl)pyrimidin-5- pure as such, yield 70%, mp: 169° C., appearance: white yl]acetamide solid 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.21 (s, 3H), 2.22 (s, 3H), 3.09-3.13 (m, 4H), 3.40 (s, 2H), 4.16-4.18 (m, 4H), 5.92 (d, 1H, J = 3.1 Hz), 5.99 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 6.10 (d, 1H, J = 8.0 Hz), 7.22-7.29 (m, 3H), 8.29 (s, 2H), 9.10 (d, 1H, J = 8.2 Hz); m/z: 489 [M + H]+ (calc. mass: 488). 50 N-[(2,4- From (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine dichlorophenyl) Ex.39 and 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5- (5-methylfuran-2- yl]acetic acid Ex.17 following protocol A, DMAP (1.2 equiv), yl)methyl]-2-[2- EDCl•HCl (1.1 equiv), overnight at rt. Sat. NH4Cl was (1,1-dioxo-1- added and the precipitate was collected by filtration and thiomorpholin-4- washed with water. The title compound was pure as such, yl)pyrimidin-5- yield 85%, mp: 215° C., appearance: white solid yl]acetamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.22 (s, 3H), 3.10-3.12 (m, 4H), 3.42 (s, 2H), 4.16-4.19 (m, 4H), 5.90 (d, 1H, J = 2.9 Hz), 6.00 (d, 1H, J = 2.2 Hz), 6.28 (d, 1H, J = 7.5 Hz), 7.44-7.52 (m, 2H), 7.61 (d, 1H, J = 1.8 Hz), 8.29 (s, 2H), 9.21 (d, 1H, J = 8.0 Hz); m/z: 509 [M + H]+, 511 [M + H]+ (calc. mass: 508). 51 N-[(2-chloro-4- From (2-chloro-4-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.40 and 2-[2-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)pyrimidin-5-yl]acetic acid Ex.17 following protocol A, yl)methyl]-2-[2- DMAP (1.2 equiv), EDCl•HCl (1.1 equiv), overnight at rt. (1,1-dioxo-1- Sat. NH4Cl was added and the precipitate was collected by thiomorpholin-4- filtration and washed with water. The title compound was yl)pyrimidin-5- pure as such, yield 84%, mp: 208° C., appearance: white yl]acetamide solid 1H NMR (300 MHz, DMSO-d6, d in ppm): 2.21 (s, 3H), 2.28 (s, 3H), 3.09-3.13 (m, 4H), 3.41 (s, 2H), 4.16-4.18 (m, 4H), 5.83 (d, 1H, J = 3.0 Hz), 5.98 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.29 (d, 1H, J = 8.2 Hz), 7.18 (d, 1H, J = 7.9 Hz), 7.26 (s, 1H), 7.32 (d, 1H, J = 7.9 Hz), 8.30 (s, 2H), 9.12 (d, 1H, J = 8.1 Hz); m/z: 511 [M + Na]+ (calc. mass: 488). 52 N-[(2-chloro-4- From (2-chloro-4-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.40 and 1-[2-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Ex.37 yl)methyl]-1-[2- following protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), (1,1-dioxo-1- 2 h at rt, purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 50:50), yield 44%, mp: 98° C., yl)pyrimidin-5- appearance: white solid yl]cyclopropane- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.92-1.05 (m, 1-carboxamide 2H), 1.3-1.42 (m, 2H), 2.19 (s, 3H), 2.28 (s, 3H), 3.08-3.15 (m, 4H), 4.18-4.24 (m, 4H), 5.66 (d, 1H, J = 3.0 Hz), 5.93 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 6.37 (d, 1H, J = 8.0 Hz), 7.14 (dd, 1H, J = 8.3 Hz, J = 1.0 Hz), 7.25-7.28 (m, 2H), 8.23 (d, 1H, J = 8.3 Hz), 8.36 (s, 2H); m/z: 537 [M + Na]+, 539 [M + Na]+ (calc. mass: 514). 53 N-[(4-chloro-2- From (4-chloro-2-methylphenyl)(5-methylfuran-2- methylphenyl)(5- yl)methanamine Ex.38 and 1-[2-(1,1-dioxo-1-thiomorpholin- methylfuran-2- 4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Ex.37 yl)methyl]-1-[2- following protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), (1,1-dioxo-1- 2 h at rt, purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 50:50), yield 49%, mp: 162° C., yl)pyrimidin-5- appearance: white solid yl]cyclopropane- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.94-1.05 (m, 1-carboxamide 2H), 1.25-1.40 (m, 2H), 2.19 (s, 3H), 2.20 (s, 3H), 3.10-3.14 (m, 4H), 4.18-4.23 (m, 4H), 5.74 (d, 1H, J = 3.0 Hz), 5.95 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.18 (d, 1H, J = 8.0 Hz), 7.16-7.25 (m, 3H), 8.24 (d, 1H, J = 8.1 Hz), 8.35 (s, 2H); m/z: 537 [M + Na]+, 539 [M + Na]+ (calc. mass: 514). 54 N-[(2,4- From (2,4-dichlorophenyl)(5-methylfuran-2-yl)methanamine dichlorophenyl) Ex.39 and 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5- (5-methylfuran-2- yl]cyclopropane-1-carboxylic acid Ex.37 following protocol yl)methyl]-1-[2- A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), 2 h at rt, (1,1-dioxo-1- purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 50:50), yield 47%, mp: 145° C., yl)pyrimidin-5- appearance: white solid yl]cyclopropane- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.95-1.05 (m, 1-carboxamide 2H), 1.30-1.42 (m, 2H), 2.20 (s, 3H), 3.1-3.15 (m, 4H), 4.19- 4.24 (m, 4H), 5.71 (d, 1H, J = 3.1 Hz), 5.96 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.37 (d, 1H, J = 7.9 Hz), 7.40 (d, 1H, J = 8.4 Hz), 7.46 (dd, 1H, J = 8.4 Hz, J = 2.0 Hz), 7.59 (d, 1H, J = 2.0 Hz), 8.33 (d, 1H, J = 8.2 Hz), 8.37 (s, 2H); m/z: 557 [M + Na]+, 559 [M + Na]+ (calc. mass: 534). 55 1-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 1-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-{[4- 4-yl)phenyl]cyclobutane-1-carboxylic acid Ex.33 following methyl-2- protocol A, DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), (piperidin-1- overnight at rt, purification by column chromatography on yl)phenyl](5- silica gel (Cyclohexane/EtOAc, 60:40). The compound was methylfuran-2- not pure enough an a second purification by column yl)methyl} chromatography on silica gel (Cyclohexane/EtOAc, 70:30) cyclobutane-1- was proceed, yield 43%, mp: 87° C., appearance: white solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.43-1.56 (m, 6H), 1.70-1.78 (m, 2H), 2.11 (s, 3H), 2.23 (s, 3H), 2.26-2.34 (m, 2H), 2.44-2.49 (m, 2H), 2.56-2.72 (m, 4H), 3.05-3.07 (m, 4H), 3.74-3.76 (m, 4H), 5.60 (d, 1H, J = 2.4 Hz), 5.86 (dd, 1H, J = 2.9 Hz, J = 1.0 Hz), 6.40 (d, 1H, J = 8.3 Hz), 6.79 (d, 1H, J = 7.1 Hz), 6.92 (s, 1H), 6.95-7.01 (m, 3H), 7.25 (d, 2H, J = 8.8 Hz), 7.98 (d, 1H, J = 8.5 Hz); m/z: 576 [M + H]+ (calc. mass: 575). 56 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-2- 4-yl)phenyl]-2-methylpropanoic acid Ex.32 following methyl-N-{[4- protocol A, DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), methyl-2- overnight at rt, purification by column chromatography on (piperidin-1- silica gel (Cyclohexane/EtOAc, 60:40), yield 53%, mp: yl)phenyl](5- 87° C., appearance: off-white solid methylfuran-2- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.40-1.45 (m, yl)methyl} 12H), 2.12 (s, 3H), 2.23 (s, 3H), 2.45-2.48 (m, 2H), 2.64- propanamide 2.70 (m, 2H), 3.07 (t, 4H, J = 5.1 Hz), 3.73 (t, 4H, J = 5.0 Hz), 5.69 (d, 1H, J = 2.3 Hz), 5.89 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.42 (d, 1H, J = 8.5 Hz), 6.83 (d, 1H, J = 6.9 Hz), 6.94-6.97 (m, 3H), 7.08 (d, 1H, J = 7.8 Hz), 7.18 (d, 2H, J = 8.9 Hz), 7.71 (d, 1H, J = 8.5 Hz); m/z: 564 [M + H]+ (calc. mass: 563). 57 1-[2-(1,1-dioxo-1- From (4-methoxy-2-methylphenyl)(5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.34 and 1-[2-(1,1-dioxo-1-thiomorpholin- yl)pyrimidin-5-yl]- 4-yl)pyrimidin-5-yl]cyclopropane-1-carboxylic acid Ex.37 N-[(4-methoxy-2- following protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), methylphenyl)(5- 2 h at rt. Sat. NH4Cl was added and the precipitate was methylfuran-2- collected by filtration and washed with water. The title yl)methyl] compound was pure as such, yield 50%, mp: 101° C., cyclopropane-1- appearance: white solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.95-1.02 (m, 2H), 1.23-1.39 (m, 2H), 2.18 (s, 3H), 2.19 (s, 3H), 3.10-3.15 (m, 4H), 3.71 (s, 3H), 4.18-4.23 (m, 4H), 5.71 (d, 1H, J = 3.1 Hz), 5.94 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.16 (d, 1H, J = 8.3 Hz), 6.68-7.72 (m, 2H), 7.05 (d, 1H, J = 8.8 Hz), 8.08 (d, 1H, J = 8.3 Hz), 8.35 (s, 2H); m/z: 533 [M + Na]+ (calc. mass: 510). 58 1-[3-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 1-[3-(1,1-dioxo-1-thiomorpholin- yl)phenyl]-N-{[4- 4-yl)phenyl]cyclopropane-1-carboxylic acid Ex.41 following methyl-2- protocol A, DMAP (2.2 equiv), EDCl•HCl (1.2 equiv), (piperidin-1- overnight at rt, purification by column chromatography on yl)phenyl](5- silica gel (Cyclohexane/EtOAc, 70:30), yield 50%, mp: methylfuran-2- 82° C., appearance: white solid yl)methyl} 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.01 (d, 2H, cyclopropane-1- J = 2.1 Hz), 1.23-1.40 (m, 8H), 2.12 (s, 3H), 2.23 (s, 3H), carboxamide 2.43-2.46 (m, 2H), 2.56-2.65 (m, 2H), 3.05-3.07 (m, 4H), 3.73-3.75 (m, 4H), 5.80 (d, 1H, J = 2.9 Hz), 5.92 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.38 (d, 1H, J = 8.6 Hz), 6.83 (d, 1H, J = 7.7 Hz), 6.87 (d, 1H, J = 9.3 Hz), 6.92-7.02 (m, 4H), 7.14 (d, 1H, J = 8.7 Hz), 7.22 (t, 1H, J = 7.7 Hz); m/z: 562 [M + H]+ (calc. mass: 561). 59 1-[4-(1,1-dioxo-1- From 3-methyl-1-[2-(piperidin-1-yl)phenyl]butan-1-amine thiomorpholin-4- Ex.54 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- yl)phenyl]-N-[3- yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following methyl-1-[2- protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), (piperidin-1- overnight at rt, purification by column chromatography on yl)phenyl]butyl] silica gel (Cyclohexane/EtOAc, 70:30), yield 55%, mp: cyclopropane-1- 91° C., appearance: white solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.83 (d, 3H, J = 11.1 Hz), 0.85 (d, 3H, J = 11.2 Hz), 0.87-0.93 (m, 2H), 1.18- 1.39 (m, 5H), 1.45-1.66 (m, 6H), 2.39-2.45 (m, 2H), 2.94- 3.05 (m, 2H), 3.06-3.14 (m, 4H), 3.73-3.82 (m, 4H), 5.24- 5.31 (m, 1H), 6.68 (d, 1H, J = 8.3 Hz), 7.00-7.06 (m, 3H), 7.06-7.11 (m, 1H), 7.11-7.17 (m, 2H), 7.22 (d, 2H, J = 8.9 Hz); m/z: 524 [M + H]+ (calc. mass: 523). 60 1-[4-(1,1-dioxo-1- From (5-methylfuran-2-yl)[2-(piperidin-1- thiomorpholin-4- yl)phenyl]methanamine Ex.42 and 1-[4-(1,1-dioxo-1- yl)phenyl]-N-[(5- thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxylic acid methylfuran-2- Ex.28 following protocol A, DMAP (1.1 equiv), EDCl•HCl (1 yl)[2-(piperidin-1- equiv), 2 h at rt, purification by column chromatography on yl)phenyl]methyl] silica gel (Cyclohexane/EtOAc, 60:40), yield 59%, mp: cyclopropane-1- 90° C., appearance: white solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.89-1 (m, 2H), 1.22-1.27 (m, 2H), 1.29-1.41 (m, 6H), 2.12 (s, 3H), 2.42- 2.50 (m, 2H), 2.56-2.65 (m, 2H), 3.05-3.12 (m, 4H), 3.73- 3.79 (m, 4H), 5.82 (d, 1H, J = 3.1 Hz), 5.92 (dd, 1H, J = 3.0 Hz, J = 1.0 Hz), 6.38 (d, 1H, J = 8.5 Hz), 7.01 (d, 2H, J = 8.8 Hz), 7.06-7.23 (m, 4H), 7.22-7.27 (m, 1H), 7.26 (d, 2H, J = 8.7 Hz); m/z: 548 [M + H]+ (calc. mass: 547). 61 2-[4-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[4-(1,1-dioxo-1-thiomorpholin- yl)-3- 4-yl)-3-hydroxyphenyl]acetic acid Ex.43 following protocol hydroxyphenyl]- A, DMAP (1.2 equiv), EDCl•HCl (1.2 equiv), overnight at rt, N-{[4-methyl-2- purification on preparative HPLC, yield 9%, mp: 105° C., (piperidin-1- appearance: white solid yl)phenyl](5- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.39-1.60 (m, methylfuran-2- 6H), 2.17 (s, 3H), 2.25 (s, 3H), 2.56-2.60 (m, 2H), 2.75-2.81 yl)methyl}acetamide (m, 2H), 3.21-3.30 (m, 8H), 5.81 (d, 1H, J = 2.9 Hz), 5.92 (d, 1H, J = 3.1 Hz), 6.46 (d, 1H, J = 8.9 Hz), 6.62 (dd, 1H, J = 7.6 Hz, J = 2.1 Hz), 6.73 (d, 1H, J = 2.1 Hz), 6.86-6.95 (m, 3H), 7.17 (d, 1H, J = 7.9 Hz), 8.66 (d, 1H, J = 8.4 Hz), 8.89 (s, 1H); m/z: 552 [M + H]+ (calc. mass: 551). 62 2-[3-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[3-(1,1-dioxo-1-thiomorpholin- yl)-4- 4-yl)-4-(methoxymethyl)phenyl]acetic acid Ex.44 following (methoxymethyl) Protocol A, DMAP (1.2 equiv), EDCl•HCl (1.1 equiv), phenyl]-N-{[4- overnight at rt, purification on preparative HPLC, yield 25%, methyl-2- mp: 87° C., appearance: white solid (piperidin-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.39-1.59 (m, yl)phenyl](5- 6H), 2.17 (s, 3H), 2.25 (s, 3H), 2.55-2.59 (m, 2H), 2.73-2.82 methylfuran-2- (m, 2H), 3.20-3.30 (m, 8H), 3.31 (s, 3H), 3.43 (d, 2H, yl)methyl}acetamide J = 3.1 Hz), 4.43 (s, 2H), 5.81 (d, 1H, J = 3.1 Hz), 5.92 (dd, 1H, J = 3.2 Hz, J = 1.1 Hz), 6.49 (d, 1H, J = 8.5 Hz), 6.90 (d, 1H, J = 7.5 Hz), 6.94 (s, 1H), 6.97 (dd, 1H, J = 7.6 Hz, J = 1.7 Hz), 7.10 (d, 1H, J = 1.4 Hz), 7.20 (d, 1H, J = 7.9 Hz), 7.25 (d, 1H, J = 7.7 Hz), 8.76 (d, 1H, J = 8.6 Hz); m/z: 580 [M + H]+ (calc. mass: 579). 63 2-[3-(1,1-dioxo-1- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[3-(1,1-dioxo-1-thiomorpholin- yl)-4- 4-yl)-4-(hydroxymethyl)phenyl]acetic acid Ex.45 following (hydroxymethyl) protocol A, DMAP (1.1 equiv), EDCl•HCl (1.1 equiv), phenyl]-N-{[4- overnight at rt, purification on preparative HPLC, yield 8%, methyl-2- mp: 100° C., appearance: white solid (piperidin-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.42-1.59 (m, yl)phenyl](5- 6H), 2.17 (s, 3H), 2.25 (s, 3H), 2.55-2.59 (m, 2H), 2.74-2.82 methylfuran-2- (m, 2H), 3.20-3.28 (m, 8H), 3.42 (d, 2H, J = 3.2 Hz), 4.51 (d, yl)methyl}acetamide 2H, J = 5.3 Hz), 5.02 (t, 1H, J = 5.7 Hz), 5.81 (d, 1H, J = 2.9 Hz), 5.90-5.95 (m, 1H), 6.48 (d, 1H, J = 9.1 Hz), 6.89 (d, 1H, J = 8.3 Hz), 6.91 (s, 1H), 6.97 (dd, 1H, J = 8.5 Hz, J = 1.5 Hz), 7.06 (d, 1H, J = 1.1 Hz), 7.21 (d, 1H, J = 7.8 Hz), 7.31 (d, 1H, J = 7.7 Hz), 8.75 (d, 1H, J = 8.3 Hz); m/z: 566 [M + H]+ (calc. mass: 565). 64 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- (5-methylfuran-2- yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following yl)methyl]-1-[4- protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), 2 h at rt, (1,1-dioxo-1- purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 70:30), yield 60%, mp: 75° C., yl)phenyl] appearance: white solid cyclopropane-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.89-0.99 (m, carboxamide 2H), 1.24-1.34 (m, 2H), 2.14 (s, 3H), 2.16 (s, 3H), 2.22 (s, 3H), 3.07-3.1 (m, 4H), 3.76 (m, 4H), 5.78 (d, 1H, J = 2.7 Hz), 5.93 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.08 (d, 1H, J = 8.3 Hz), 6.86-6.92 (m, 2H), 6.95 (s, 1H), 7.00 (d, 2H, J = 8.9 Hz), 7.04 (d, 1H, J = 8.4 Hz), 7.24 (d, 2H, J = 8.8 Hz); m/z: 515 [M + Na]+ (calc. mass: 492). 65 2-[5-(1,1-dioxo-1-4- From [4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2- thiomorpholin-4- yl)methanamine Ex.6 and 2-[5-(1,1-dioxo-1-thiomorpholin- yl)pyrimidin-2-yl]- yl)pyrimidin-2-yl]acetic acid Ex.46 following protocol A, N-{[4-methyl-2- DMAP (1 equiv), EDCl•HCl (1.1 equiv), 2 h at rt, purification (piperidin-1- by column chromatography on silica gel (CH2Cl2/MeOH, yl)phenyl](5- 95:5), yield 18%, mp: 99° C., appearance: pale brown solid methylfuran-2- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.39-1.63 (m, yl)methyl}acetamide 6H), 2.18 (s, 3H), 2.26 (s, 3H), 2.54-2.63 (m, 2H), 2.76-2.89 (m, 2H), 3.09-3.22 (m, 4H), 3.64-3.76 (m, 2H), 3.77-3.88 (m, 4H), 5.89-5.96 (m, 2H), 6.49 (d, 1H, J = 8.5 Hz), 6.91 (d, 1H, J = 8.1 Hz), 6.95 (s, 1H), 7.22 (d, 1H, J = 7.7 Hz), 8.49 (s, 2H), 8.76 (d, 1H, J = 8.2 Hz); m/z: 538 [M + H]+ (calc. mass: 537). 66 N-[(5-chlorofuran- From (5-chlorofuran-2-yl)(2,4-dimethylphenyl)methanamine 2-yl)(2,4- Ex.47 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- dimethylphenyl) yl)phenyl]cyclopropane-1:carboxylic acid Ex.28 following methyl]-1-[4-(1,1- protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), dioxo-1- overnight at rt. Sat. NH4Cl was added and the precipitate thiomorpholin-4- was collected by filtration and washed with water. The title yl)phenyl] compound was pure as such, yield 71%, mp: 76° C., cyclopropane-1- appearance: pale yellow solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.89-1.02 (m, 2H), 1.24-1.34 (m, 2H), 2.15 (s, 3H), 2.22 (s, 3H), 3.03-3.14 (m, 4H), 3.70-3.82 (m, 4H), 6.02 (dd, 1H, J = 3.3 Hz, J = 1.0 Hz), 6.13 (d, 1H, J = 8.2 Hz), 6.35 (d, 1H, J = 3.3 Hz), 6.89-6.96 (m, 3H), 6.99 (d, 2H, J = 9.1 Hz), 7.23 (d, 2H, J = 8.7 Hz), 7.39 (d, 1H, J = 8.2 Hz); m/z: 535 [M + Na]+, 537 [M + Na]+ (calc. mass: 512). 67 N-[(5-chlorofuran- From (5-chlorofuran-2-yl)(4-methylphenyl)methanamine 2-yl)(4- Ex.48 and 1-[4-(1,1-dioxo-1-thiomorpholin-4- methylphenyl) yl)phenyl]cyclopropane-1-carboxylic acid Ex.28 following methyl]-1-[4-(1,1- protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), dioxo-1- overnight at rt. Sat. NH4Cl was added and the precipitate thiomorpholin-4- was collected by filtration and washed with water. The title yl)phenyl] compound was pure as such, yield 71%, mp: 157° C., cyclopropane-1- appearance: white solid carboxamide 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.90-1.01 (m, 2H), 1.24-1.35 (m, 2H), 2.26 (s, 3H), 3.02-3.15 (m, 4H), 3.70-3.84 (m, 4H), 6.03 (d, 1H, J = 8.6 Hz), 6.08 (dd, 1H, J = 3.3 Hz, J = 0.9 Hz), 6.35 (d, 1H, J = 3.3 Hz), 7.00 (d, 2H, J = 8.8 Hz), 7.08 (d, 2H, J = 8.3 Hz), 7.13 (d, 2H, J = 8.3 Hz), 7.24 (d, 2H, J = 8.7 Hz), 7.37 (d, 1H, J = 8.4 Hz); m/z: 521 [M + Na]+, 523 [M + Na]+ (calc. mass: 498). 68 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[3-(1,1-dioxo-1-thiomorpholin-4- (5-methylfuran-2- yl)phenyl]cyclopropane-1-carboxylic acid Ex.41 following yl)methyl]-1-[3- protocol A, DMAP (1 equiv), EDCl•HCl (1.1 equiv), 2 h at rt, (1,1-dioxo-1- purification by column chromatography on silica gel thiomorpholin-4- (Cyclohexane/EtOAc, 50:50), yield 42%, mp: 72° C., yl)phenyl] appearance: white solid cyclopropane-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.96-1.10 (m, carboxamide 2H), 1.22-1.35 (m, 2H), 2.15 (s, 3H), 2.16 (s, 3H), 2.22 (s, 3H), 3.05-3.13 (m, 4H), 3.72-3.80 (m, 4H), 5.75 (d, 1H, J = 3.1 Hz), 5.93 (dd, 1H, J = 3.1 Hz, J = 1.1 Hz), 6.12 (d, 1H, J = 8.5 Hz), 6.81 (d, 1H, J = 8.0 Hz), 6.90-7.01 (m, 5H), 7.22 (t, 1H, J = 7.9 Hz), 7.29 (d, 1H, J = 8.4 Hz); m/z: 515 [M + Na]+ (calc. mass: 492). 69 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4- (5-methylfuran-2- methoxyphenyl]cyclopropane-1-carboxylic acid Ex.49 yl)methyl]-1-[3- following protocol A, DMAP (1.1 equiv), EDCl•HCl (1.2 (1,1-dioxo-1- 2-equiv): overnight at rt. Sat. NH4Cl was added and the thiomorpholin-4- precipitate was collected by filtration and washed with yl)-4- water. The title compound was pure as such, yield 70%, methoxyphenyl] mp: 174° C., appearance: white solid cyclopropane-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.91-1.06 (m, carboxamide 2H), 1.21-1.33 (m, 2H), 2.16 (s, 6H), 2.22 (s, 3H), 3.17-3.26 (m, 4H), 3.34-3.42 (m, 4H), 3.79 (s, 3H), 5.75 (d, 1H, J = 2.9 Hz), 5.93 (dd, 1H, J = 3.1 Hz, J = 1.0 Hz), 6.11 (d, 1H, J = 8.3 Hz), 6.87-7.03 (m, 6H), 7.20 (d, 1H, J = 8.3 Hz); m/z: 545 [M + Na]+ (calc. mass: 522). 70 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2- (5-methylfuran-2- methylphenyl]cyclopropane-1-carboxylic acid Ex.50 yl)methyl]-1-[5- following protocol A, DMAP (1.1 equiv), EDCl•HCl (1.2 (1,1-dioxo-1- equiv), overnight at rt. Sat. NH4Cl was added and the thiomorpholin-4- precipitate was collected by filtration and washed with yl)-2- water. The title compound was pure as such, yield 72%, methylphenyl] mp: 86° C., appearance: white solid cyclopropane-1- 1H NMR (300 MHz, DMSO-d6, d in ppm): 0.91-1.10 (m, carboxamide 2H), 1.29-1.51 (m, 2H), 2.15-2.17 (m, 9H), 2.22 (s, 3H), 3.03-3.14 (m, 4H), 3.70-3.80 (m, 4H), 5.69 (d, 1H, J = 3.1 Hz), 5.92 (dd, 1H, J = 3.0 Hz, J = 1.1 Hz), 6.13 (d, 1H, J = 8.4 Hz), 6.82 (d, 1H, J = 8.3 Hz), 6.85-6.96 (m, 4H), 6.98 (d, 1H, J = 2.6 Hz), 7.09 (d, 1H, J = 8.6 Hz); m/z: 529 [M + Na]+ (calc. mass: 506). 71 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6- (5-methylfuran-2- methylpyridin-2-yl]cyclopropane-1-carboxylic acid Ex.51 yl)methyl]-1-[5- following protocol A, DMAP (1.1 equiv), EDCl•HCl (1.1 (1,1-dioxo-1- equiv), overnight at rt, purification on preparative HPLC, thiomorpholin-4- yield 37%, mp: 74° C., appearance: white solid yl)-6- 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.13-1.20 (m, methylpyridin-2- 2H), 1.37-1.48 (m, 2H), 2.20 (s, 3H), 2.23 (s, 3H), 2.24 (s, yl]cyclopropane- 3H), 2.45 (s, 3H), 3.26-3.30 (m, 8H), 5.94 (d, 1H, J = 3.2 Hz), 1-carboxamide 5.96 (dd, 1H, J = 3.0 Hz, J = 0.9 Hz), 6.18 (d, 1H, J = 8.1 Hz), 6.95-7.00 (m, 2H), 7.02 (d, 1H, J = 8.3 Hz), 7.12 (d, 1H, J = 8.4 Hz), 7.50 (d, 1H, J = 8.5 Hz), 10.08 (d, 1H, J = 8.1 Hz); m/z: 508 [M + H]+ (calc. mass: 507). 72 N-[(2,4- From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3- (5-methylfuran-2- methylpyridin-2-yl]cyclopropane-1-carboxylic acid Ex.52 yl)methyl]-1-[5- following protocol A, DMAP (2.1 equiv), EDCl•HCl (2.1 (1,1-dioxo-1- equiv), overnight at rt. Sat. NH4Cl was added and the thiomorpholin-4- precipitate was collected by filtration and washed with yl)-3- water. The solid was redissolved with EtOAc. The organic methylpyridin-2- layer was washed with water, partitionated, dried over yl]cyclopropane- MgSO4, filtered and the solution was concentrated to 1-carboxamide dryness. The title compound was pure as such, yield 43%, mp: 87° C., appearance: white solid 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.00-1.15 (m, 2H), 1.33-1.44 (m, 2H), 2.16 (s, 6H), 2.18 (s, 3H), 2.22 (s, 3H), 3.07-3.17 (m, 4H), 3.75-3.86 (m, 4H), 5.68 (d, 1H, J = 3.0 Hz), 5.92 (dd, 1H, J = 2.9 Hz, J = 1.1 Hz), 6.20 (d, 1H, J = 8.3 Hz), 6.89-6.98 (m, 3H), 7.24-7.34 (m, 2H), 8.11 (d, 1H, J = 2.9 Hz); m/z: 508 [M + H]+ (calc. mass: 507). 73 N-[(2,4- (From (2,4-dimethylphenyl)(5-methylfuran-2-yl)methanamine dimethylphenyl) Ex.20 and 1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2- 5-methylfuran-2- yl]cyclopropane-1-carboxylic acid Ex.53 following protocol yl)methyl]-1-[5- A, DMAP (2.1 equiv), EDCl•HCl (2.1 equiv), overnight at rt. (1,1-dioxo-1- Sat. NH4Cl was added and the precipitate was collected by thiomorpholin-4- filtration and washed with water. The solid was redissolved yl)pyridin-2- with EtOAc. The organic layer was washed with water, yl]cyclopropane- partitionated, dried over MgSO4, filtered and the solution 1-carboxamide was concentrated to dryness. The title compound was pure as such, yield 59%, mp: 71° C., appearance: white solid 1H NMR (300 MHz, DMSO-d6, d in ppm): 1.11-1.20 (m, 2H), 1.29-1.39 (m, 2H), 2.19 (s, 3H), 2.22 (s, 3H), 2.23 (s, 3H), 3.08-3.18 (m, 4H), 3.75-3.86 (m, 4H), 5.86 (d, 1H, J = 3.0 Hz), 5.95 (dd, 1H, J = 2.9 Hz, J = 0.9 Hz), 6.21 (d, 1H, J = 8.9 Hz), 6.93-7.01 (m, 2H), 7.07 (d, 1H, J = 8.2 Hz), 7.14 (d, 1H, J = 8.7 Hz), 7.41 (dd, 1H, J = 8.5 Hz, J = 2.9 Hz), 8.31 (d, 1H, J = 2.8 Hz), 9.20 (d, 1H, J = 8.3 Hz); m/z: 494 [M + H]+ (calc. mass: 493).

Example 3: RORE Luciferase/RORvt Transactivation Assay

It is well known that RORγ binds to a conserved non-coding sequence (CNS) enhancer element in the IL-17 promoter. Accordingly, we have used in this assay a luciferase reporter gene construct that contains the human IL-17 promoter fragment with RORγ-specific CNS enhancer element and a RORγt overexpressing plasmid, to indirectly assess the effect of compounds on RORγ activity. Inhibition of RORγ activity by test compounds will result in a decrease in luciferase activity in COS-7 cells transfected with the reporter construct.

COS-7 Cell Line Culture

Monkey Kidney COS-7 cell line are maintained in a standard culture medium Dulbecco's modified Eagle's minimal (DMEM) medium supplemented with 10% fetal calf serum, 1% sodium pyruvate, 1% essential amino acids and 1% antibiotics at 37° C. in a humidified atmosphere of 5% CO2 and 95% air. Culture medium was changed every 2 days.

Construct Descriptions

The 4.3 Kb human IL-17 promoter containing the RORγ-specific CNS enhancer element was PCR amplified from human genomic DNA and cloned into a pGL3-TKLuc2Cp reporter plasmid. To overexpress RORγt, the full-length cDNA of human RORγt (identical to published sequence NM 001001523) was cloned without any restriction into pcdna3.1DV5-His-topo to generate the RORγt overexpression plasmid “RORγt_FL_h_pcDNA3.1DV5-His-TOPO_1”.

COS-7 Cell Transfection

The luciferase reporter plasmid and the RORγt overexpression plasmid were transfected into COS-7 cell line using 4μL JetPEI™/μg of DNA. Briefly, 150 ng of DNA (ration 1/2 between RORE-Tk Luc2Cp and cDNA RORγt or the empty vector for the negative control) was served to transfect adherent COS-7 cells in a 225 cm3 culture flask, in complete medium (see cos-7 cell line culture). Cells were incubated for 24 hours in a humidified atmosphere of 5% CO2 and 95% air

Cells were then detached (using trypsin) and washed by centrifugation at 300 g for 10 minutes. Cell pellet was resuspended in serum free/phenol red free DMEM and seeded in 384 well plates at a density of 10000 cells/well and then incubated for 4 h at 37° C.

Assay

Compounds were dissolved in 100% DMSO to obtain 10 mM stock solutions. For each compound, test concentrations were diluted in serum free/phenol red free DMEM using the Genesis Freedom 200™ (TECAN) and added to the cells to obtain a 0.3% DMSO final concentration (in a final volume of 40 μL per well). T091317 was used as reference compound. Cells were incubated in presence of compounds for an additional 20 h at 37° C. in a humidified atmosphere of 5% CO2 and 95% air

The luciferase activity was then measured with 40 μL/well steady-Glo Luciferase assay system (Promega, Madison, Wis.) and after incubation at room temperature for 30 minutes. The luminescence was estimated using the Ultra384 reader (TECAN). Data were collected and analyzed using GraphPad Prism software (GraphPad Software V5.02, San Diego Calif. USA). IC50 in μM and Emax in % were reported for each compound.

Results:

Effect of reference compound on RORγt activity: in this assay, reference compound T091317 showed on RORγt activity inhibition with IC₅₀ of 0.2 μM and an Emax of 83.7%

Several compounds belonging to formula (I) or (Ia) inhibit the high transcriptional activity of RORγ at different levels. These compounds displayed an IC₅₀ comprised between 1 and 10 μM in particular Cpds. 2, 4, 7-8, 17, 24, 33, 35, 42, 43, 50, 52, and 59. Cpds. 1, 5, 9-11, 13-16, 25-26, 28-30, 34, 36, 40-41, 45, 54-58, 60, 62-64, 68, and 73 displayed an IC₅₀ comprised between 0.1 and 1 μM. Best compounds (such as Cpds. 6, 12, 18-23, 27, 31-32, 37-39, 44, 46-49, 53, 61, 65-67, and 71-72) displayed an IC₅₀ inferior to 0.1 μM.

Further, the major part of compounds from this chemical series showed no cytotoxic effect at 30 μM as judged from the reporter signal obtained from cells transfected with the empty vector that was used as negative control in this experiment.

Example 4: FRET General Considerations

Time-resolved FRET (TR-FRET) RORγt coactivator assay was used to identify RORγ modulator compounds with ligand-dependent coactivator displacement. The assay uses a d2-labeled anti-GST antibody, synthetic N-terminally biotinylated peptide which is derived from nuclear receptor coactivator protein RIP140, and a RORγt ligand-binding domain (RORγt-LBD) that is tagged with glutathione-S-transferase (GST). The influence of compounds on the RORγ-peptide interaction relies on the binding dependent energy transfer from a donor to an acceptor fluorophor attached to the binding partner of interest. Because RORγ is constitutively active, streptavidin-terbium conjugate labeled-coactivator peptide is recruited in the absence of ligand and the terbium d2 on the anti-GST antibody is excited at 340 nm, energy is transferred to the terbium label on the coactivator peptide and detected as emission at 665 nm. For reduction of background from compound fluorescence, TR-FRET method makes use of generic fluorophore labels and time resolved detection.

Assay

The assays were done in a final volume of 20 μl in a 384 well plate in a CHAPS buffer (2 mM CHAPS; 1 mM DTT, 2 mM EDTA; 0.1% BSA), containing 20 nM recombinantly expressed RORγ-LBD fused to GST, 30 nM N-terminally biotinylated peptide, 1 nM streptavidin-terbium conjugate and 20 nM d2 labeled-anti-GST. Test compounds were diluted using 10 mM stock solution. The range of the final compound concentrations used in this test was from 0.3 nM to 30 μM (logarithmic scale). DMSO content of the samples was kept at 1%. The assay was equilibrated for 2 hours in the dark at room temperature in 384 well plates (Falcon). The signal was detected by an Ultra384 reader (TECAN). The results were visualized by plotting the ratio between the emitted light at 665 nm and 620 nm. A basal level of RORγ-peptide formation is observed in the absence of added compound. Compounds that promote coactivator displacement induce a concentration-dependent decrease in time-resolved fluorescent signal. Data were collected and analyzed using GraphPad Prism software (GraphPad Software V5.02, San Diego Calif. USA). IC50 in μM and Emax in % were reported for each compound.

Results:

Effect of reference compound on RORγt activity: in this assay, reference compound T091317 showed on RORγt activity inhibition with IC₅₀ of 0.097 μM and an Emax of 37%

Several compounds belonging to formula (I) or (Ia) inhibit the ligand-dependent coactivator-RORγt binding.

Cpds 2, 42, 51, and 64 displayed an IC₅₀ comprised between 1 and 10 μM. Cpds 4-5, 7-8, 10, 13-14, 17, 23-24, 30, 32, 34-35, 37, 46, 55-56, 59, and 70 displayed an IC₅₀ comprised between 0.1 μM and 1 μM. Best compounds (such as Cpds. 1, 6, 9, 11-12, 15-16, 18-22, 25-29, 31, 36, 38-41, 43-45, 47-48, 52-54, 58, 60, 65-68, and 71) displayed an IC₅₀ inferior to 1 μM.

Example 5: IL-17 Secretion from EL4 Murine Lymphoma

Murine EL-4 lymphoma cell line overexpressing human RORγt was used in this functional assay to assess compound ability to inhibit IL-17 cytokine secretion.

EL-4 Cell Transfection

EL-4 cells are maintained in a standard culture medium RPMI supplemented with 10% fetal calf serum, 1% sodium pyruvate, 1% essential amino acids and 1% antibiotics at 37° C. in a humidified atmosphere of 5% CO2 and 95% air. Culture medium was changed every 2 days. EL4 cells were transfected with a plasmid encoding hRORγt (sequence identical to published sequence NM 001001523). Transfection of EL4 cells was achieved with Amaxa electroporation apparatus (Amaxa Biosystems, Germany), as per the manufacturer's protocols, for the EL4 cells (Amaxa Cell Line Nucleofector Kit L, Amaxa Biosystems). Briefly, 1 μg of DNA/1 million cells was served to transfect EL-4 cells. Cell/DNA suspension was transferred into certified cuvette and the electroporation of RORγt plasmid was carried out using appropriate Nucleofector® program.

IL-17 Secretion Assay

Cells were seeded in 96 well plates at a density of 150000 cells/well then treated with compounds of this invention at indicated concentrations and incubated for 24 hours at 37° C. in a humidified atmosphere of 5% CO2 and 95% air. EL-4 cells were pretreated with test compounds (RORγ modulators) and stimulated with PMA (10 ng/mL) and ionomycin (1 μM final concentration) in the presence of test compound concentrations for additional 24 h at 37° C. in a humidified atmosphere of 5% CO2 and 95% air. Subsequently, supernatants were collected (after centrifugation at 300 g for 10 minutes) to determine the concentrations of IL-17 by HTRF (CisBio, France) or ELISA (R&D Systems Europe) according to the manufacturer's protocols.

Results:

Many of the compounds listed above were evaluated for IL-17 secretion inhibition in human RORγt-transfected EL4 Tcells. Data from this assay correlate with the activity observed in RORE Tk luc/RORγt assay.

Cpds 57 and 70 displayed an IC₅₀ comprised between 1 and 10 μM.

Cpd. 1, 5, 9-11, 13, 21-23, 25, 28, 52-54, 59, and 71 displayed an IC50 comprised between 0.1 μM and 1 μM.

Best compounds (such as Cpds. 6, 12, 15-16, 18-20, 27, 31-32, 38-39, 46, 48, 60, 66, and 72) displayed an IC₅₀ inferior to 1 μM.

REFERENCES

-   Armarego W L F, Chai C L L (2009) Purification of Laboratory     Chemicals (Sixth Edition): ELSEVIER. -   Asada M, Obitsu T, Nagase T, Tanaka M, Yamaura Y, Takizawa H,     Yoshikawa K, Sato K, Narita M, Ohuchida S, Nakai H, Toda M (2010)     3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and     selective EP3 receptor antagonists. Part 1: discovery and     exploration of the carboxyamide side chain. Bioorg Med Chem 18:     80-90 -   Bauer M (2004) Polymorphisme et stabilité, Paris, FRANCE: Editions     de sante. -   Crispín J C, Oukka M, Bayliss G, Cohen R A, Van Beek C A, Stillman I     E, Kyttaris V C, Juang Y-T, Tsokos G C (2008) Expanded Double     Negative T Cells in Patients with Systemic Lupus Erythematosus     Produce IL-17 and Infiltrate the Kidneys. The Journal of Immunology     181: 8761-8766 -   Dang Eric V, Barbi J, Yang H-Y, Jinasena D, Yu H, Zheng Y, Bordman     Z, Fu J, Kim Y, Yen H-R, Luo W, Zeller K, Shimoda L, Topalian     Suzanne L, Semenza Gregg L, Dang Chi V, Pardoll Drew M, Pan F (2011)     Control of TH17/Treg Balance by Hypoxia-Inducible Factor 1. Cell     146: 772-784 -   Dubrovskiy A V, Larock R C (2012) Synthesis of o-(dimethylamino)aryl     ketones, acridones, acridinium salts, and 1H-indazoles by the     reaction of hydrazones and arynes. J Org Chem 77: 11232-11256 -   Eberl G, Marmon S, Sunshine M J, Rennert P D, Choi Y, Littman D     R (2004) An essential function for the nuclear receptor RORgamma(t)     in the generation of fetal lymphoid tissue inducer cells. Nat     Immunol 5: 64-73 -   Erdemir D, Lee A Y, Myerson A S (2007) Polymorph selection: the role     of nucleation, crystal growth and molecular modeling. Curr Opin Drug     Discov Devel 10: 746-755 -   Furuzawa-Carballeda J, Vargas-Rojas M I, Cabral A R (2007)     Autoimmune inflammation from the Th17 perspective. Autoimmunity     Reviews 6: 169-175 -   Gennaro A (2000) Remington: The Science and Practice of     Pharmacy—20th edition: Baltimore, Md.; Lippincott Williams &     Wilkins. -   Grell W, Hurnaus R, Griss G, Sauter R, Rupprecht E, Mark M, Luger P,     Nar H, Wittneben H, Muller P (1998) Repaglinide and related     hypoglycemic benzoic acid derivatives. J Med Chem 41: 5219-5246 -   He Y-W, Deftos M L, Ojala E W, Bevan M J (1998) RORγt, a Novel     Isoform of an Orphan Receptor, Negatively Regulates Fas Ligand     Expression and IL-2 Production in T Cells. Immunity 9: 797-806 -   Hirose T, Smith R J, Jetten A M (1994) ROR-γ: The Third Member of     ROR/RZR Orphan Receptor Subfamily That Is Highly Expressed in     Skeletal Muscle. Biochemical and Biophysical Research Communications     205: 1976-1983 -   Korn T, Bettelli E, Oukka M, Kuchroo V K (2009) IL-17 and Th17     Cells. Annual Review of Immunology 27: 485-517 -   Kumar L, Amin A, Bansal A K (2007) An overview of automated systems     relevant in pharmaceutical salt screening. Drug Discov Today 12:     1046-1053 -   Lipp M, Muller G (2004) Lymphoid organogenesis: getting the green     light from RORgamma(t). Nat Immunol 5: 12-14 -   Liu S-J, Tsai J-P, Shen C-R, Sher Y-P, Hsieh C-L, Yeh Y-C, Chou A-H,     Chang S-R, Hsiao K-N, Yu F-W, Chen H-W (2007) Induction of a     distinct CD8 Tnc17 subset by transforming growth factor-β and     interleukin-6. Journal of Leukocyte Biology 82: 354-360 -   Lubberts E, Koenders M I, Oppers-Walgreen B, van den Bersselaar L,     Coenen-de Roo C J J, Joosten L A B, van den Berg W B (2004)     Treatment with a neutralizing anti-murine interleukin-17 antibody     after the onset of collagen-induced arthritis reduces joint     inflammation, cartilage destruction, and bone erosion. Arthritis &     Rheumatism 50: 650-659 -   Mahato R, Narang A (2011) Pharmaceutical Dosage Forms and Drug     Delivery, Second Edition: CRC Press. -   Morissette S L, Almarsson O, Peterson M L, Remenar J F, Read M J,     Lemmo A V, Ellis S, Cima M J, Gardner C R (2004) High-throughput     crystallization: polymorphs, salts, co-crystals and solvates of     pharmaceutical solids. Adv Drug Deliv Rev 56: 275-300 -   Murdoch J R, Lloyd C M (2010) Resolution of Allergic Airway     Inflammation and Airway Hyperreactivity Is Mediated by     IL-17-producing γδT Cells. American Journal of Respiratory and     Critical Care Medicine 182: 464-476 -   Mutlib A E (2008) Application of stable isotope-labeled compounds in     metabolism and in metabolism-mediated toxicity studies. Chem Res     Toxicol 21: 1672-1689 -   Ortiz M A, Piedrafita F J, Pfahl M, Maki R (1995) TOR: a new orphan     receptor expressed in the thymus that can modulate retinoid and     thyroid hormone signals. Molecular Endocrinology 9: 1679-1691 -   Rachitskaya A V, Hansen A M, Horai R, Li Z, Villasmil R, Luger D,     Nussenblatt R B, Caspi R R (2008) Cutting Edge: NKT Cells     Constitutively Express IL-23 Receptor and RORγt and Rapidly Produce     IL-17 upon Receptor Ligation in an IL-6-Independent Fashion. Journal     of immunology (Baltimore, Md.: 1950) 180: 5167-5171 -   Reddy I K, Mehvar R (2004) Chirality in Drug Design and Development:     CRC Press. -   Robak M T, Herbage M A, Ellman J A (2010) Synthesis and applications     of tert-butanesulfinamide. Chem Rev 110: 3600-3740 -   Rowe R, Sheskey P, Weller P, Rowe R, Sheskey P, Weller P (2003)     Handbook of Pharmaceutical Excipients, 4th Edition. -   Showalter H D, Sercel A D, Leja B M, Wolfangel C D, Ambroso L A,     Elliott W L, Fry D W, Kraker A J, Howard C T, Lu G H, Moore C W,     Nelson J M, Roberts B J, Vincent P W, Denny W A, Thompson A M (1997)     Tyrosine kinase inhibitors. 6. Structure-activity relationships     among N- and 3-substituted 2,2′-diselenobis(1H-indoles) for     inhibition of protein tyrosine kinases and comparative in vitro and     in vivo studies against selected sulfur congeners. J Med Chem 40:     413-426 -   Skepner J, Ramesh R, Trocha M, Schmidt D, Baloglu E, Lobera M,     Carlson T, Hill J, Orband-Miller L A, Barnes A, Boudjelal M, Sundrud     M, Ghosh S, Yang J (2014) Pharmacologic inhibition of RORgammat     regulates Th17 signature gene expression and suppresses cutaneous     inflammation in vivo. J Immunol 192: 2564-2575 -   Solt L A, Kumar N, Nuhant P, Wang Y, Lauer J L, Liu J, Istrate M A,     Kamenecka T M, Roush W R, Vidovic D, Schurer S C, Xu J, Wagoner G,     Drew P D, Griffin P R, Burris T P (2011) Suppression of TH17     differentiation and autoimmunity by a synthetic ROR ligand. Nature     472: 491-494 -   Stahl P, Wermuth C (2002) Handbook of Pharmaceutical Salts:     Properties, Selection, and Use: Verlag Helvetica Chimica Acta,     Zurich, Switzerland, and Wiley-VCH, Weinheim, Germany. -   Stockinger B, Veldhoen M, Martin B (2007) Th17 T cells: Linking     innate and adaptive immunity. Seminars in Immunology 19: 353-361 -   Tuskey A, Behm B W (2014) Profile of ustekinumab and its potential     in patients with moderate-to-severe Crohn's disease. Clinical and     Experimental Gastroenterology 7: 173-179 -   Wuts P G M, Greene T W (2007) Greene's Protective Groups in Organic     Synthesis, Fourth Edition: John Wiley & Sons. -   Yamashita T, Iwakura T, Matsui K, Kawaguchi H, Obana M, Hayama A,     Maeda M, Izumi Y, Komuro I, Ohsugi Y, Fujimoto M, Naka T, Kishimoto     T, Nakayama H, Fujio Y (2011) IL-6-mediated Th17 differentiation     through RORγt is essential for the initiation of experimental     autoimmune myocarditis, Vol. 91. -   Yang X O, Pappu B, Nurieva R, Akimzhanov A, Kang H S, Chung Y, Ma L,     Shah B, Panopoulos A D, Schluns K, Watowich S S, Tian Q, Jetten A M,     Dong C (2008) TH17 lineage differentiation is programmed by orphan     nuclear receptors RORα and RORγ. Immunity 28: 29-39 -   Yin S X, Grosso J A (2008) Selecting and controlling API crystal     form for pharmaceutical development—strategies and processes. Curr     Opin Drug Discov Devel 11: 771-777 

1. A compound of formula (Ia)

in which, R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, or a heterocyclic group; R1b is a hydrogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkyl group or a heterocyclic group; R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, a heterocyclic group, a cyano group, an amido group or a hydroxyl group; R1d and R1e are, independently, a hydrogen atom, a halogen atom, a (C1-C6)alkyloxy group or a (C1-C6)alkyl group; wherein at least one R1a, Rib, R1c, R1d, and R1e is not a hydrogen atom; R2 is a (C3-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group optionally substituted by a (C1-C6)alkyl group or by a halogen; R′2 is a hydrogen atom, a (C1-C6)alkyl group, a (C2-C6)alkenyl group, a (C2-C6)alkynyl group, a (C3-C14)cycloalkyl group, a (C6-C14)aryl group optionally substituted by a (C1-C6)alkyl group or a heterocyclic group, optionally substituted by a (C1-C6)alkyl group; or R2 and R′2 can form, together with the carbon atom to which they are attached, a cycloalkyl group or a heterocycloalkyl group; L1 is a NR7-CO—CH2, NR7-CO—, NR7-CO—C(CH3)2, CO—NH—CH2, CO—NH or CO—NH—C(CH3)2 group; R7 represents a hydrogen atom or a (C1-C6)alkyl group; L2 represents a bond, a (C1-C6)alkyl group, a (C3-C14)cycloalkyl group, or a CR8R′ 8 group; with the proviso that when L1 is a NR7-CO— or a CO—NH group, L2 represents a (C1-C6)alkyl group, a (C3-C14)cycloalkylgroup, or a CR8R′8 group; R8 and R′8 are independently, a hydrogen atom, or a (C1-C6)alkylgroup; R8 and R′8 can form, together with the carbon atom to which they are attached, a cycloalkyl group; X1, X2, X3, X4, X5 are, independently, a carbon, or a nitrogen atom; X6 represents a CH group or a nitrogen atom; X7 represents a sulfur atom, a SO2 group, or an oxygen atom; and R4 is a hydrogen atom; an alkyl group optionally substituted by a hydroxy group or an alkoxy group; a halogen atom; an alkyloxy group or a hydroxy group.
 2. The compound according to claim 1, wherein R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group optionally substituted by at least one halogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, a piperidinyl group, a pyrrolidinyl group, a morpholinyl, an azabicyclohexanyl group, or an azepanyl group wherein said piperidinyl, pyrrolidinyl, azepanyl, or an azabicyclohexanylgroup can be optionally substituted by at least one (C1-C6)alkyl groups.
 3. The compound according to claim 1, wherein: R1a is a hydrogen atom, a halogen atom, a nitrile group, a nitro group (NO2), a (C1-C6)alkyl group optionally substituted by at least one halogen atom, a (C1-C6)alkyloxy group, a (C1-C6)alkylthio group, an amino group, a (C1-C6)alkylamino group, a (C1-C6)dialkylamino group, a piperidinyl group, a morpholinyl group, an azabicyclohexanyl group or an azepanyl group, wherein said piperidinyl, pyrrolidinyl or azepanyl group can be optionally substituted by at least one (C1-C6)alkyl groups; R1b is a hydrogen atom; R1c is a hydrogen atom, a halogen atom, a (C1-C6)alkyl group, or a (C1-C6)alkyloxy group; and R2 is an aryl group, or a heteroaryl group, and R′2 is a hydrogen atom.
 4. The compound according to claim 1, wherein X6 is a nitrogen atom and X7 is a SO2 group or an oxygen atom.
 5. The compound according to claim 1, wherein L1 is a NR7-CO— group and L2 is a CR8R′8 group.
 6. The compound according to claim 1, wherein: R1a is a halogen atom, (such as brome), a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group, such methyl group can be substituted by halogen atom such as a trifluoromethyl group), a (C1-C6)dialkylamino group (such as dimethylamino group or diethylamino group, in particular dimethylamino group), a piperidinyl group (such as a piperidin-1-yl group), a morpholinyl group (such as a morpholin-4-yl), an azabicyclohexanyl group (such as a 3-azabicyclo[3.1.0]hexan-3-yl group) or an azepanyl group (such as a azepan-1-yl group), wherein said piperidinyl, morpholinyl, azabicyclohexanyl or azepanyl group can be optionally substituted by at least one (C1-C6)alkyl groups; R1b is a hydrogen atom; R1c is a hydrogen, a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group), or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group); R1d and R1e are hydrogen atoms; R2 is a phenyl group or a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group); L1 represents a NH—CO— group; L2 represents a CH2 group or a group of formula (III) or of formula (IV)

R4 is a hydrogen atom, a halogen atom (such as a fluor atom), a (C1-C6)alkyl group (such as a methyl group or an ethyl group, in particular a methyl group) or a (C1-C6)alkoxy group (such as a methoxy or a an ethoxy group, in particular a methoxy group); the cycle

is a substituent of X3 (in meta or para position of the L1-L2 group); and X6 is a nitrogen atom and X7 is a SO2 group or an oxygen atom.
 7. The compound according to claim 1, wherein: R1a is a heterocyclic group (in particular a piperidinyl group (such as a piperidin-1-yl group)); R1c is a (C1-C6)alkyl group (such as a methyl or ethyl group, in particular a methyl group); R2 is a heterocyclic group (such as a substituted or unsubstituted furanyl group, in particular a 5-methylfuranyl group, more particularly a 5-methylfuran-2-yl group); L1 represents a NH—CO— group; L2 represents a CH2 group R4 is a hydrogen atom; the cycle

is a substituent of X1, X2 or X3, in particular X3 (in meta or para position of the L1-L2 group); and X6 is a nitrogen atom and X7 is a SO2 group.
 8. The compound according to claim 1, characterized in that it is selected in the group consisting of: 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]-N-{phenyl[2-(piperidin-1-yl)phenyl]methyl}acetamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-fluorophenyl]-N-{[4-methyl-2-(morpholin-4-yl)phenyl](phenyl)methyl}acetamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(morpholin-4-yl)phenyl](phenyl)methyl}acetamide; 2-[2-fluoro-5-(morpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](phenyl)methyl}acetamide; N-[(2-bromo-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-{[4-methoxy-2-(4-methylpiperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]-N-({4-methoxy-2-[4-(trifluoromethyl)piperidin-1-yl]phenyl}(5-methylfuran-2-yl)methyl)acetamide; N-{[2-(dimethylamino)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methoxyphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[5-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]acetamide; N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(phenyl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylphenyl]acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}-2-[6-(morpholin-4-yl)pyridin-3-yl]acetamide; N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}-2-[2-(morpholin-4-yl)pyrimidin-5-yl]acetamide; 2-[6-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-3-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]acetamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methoxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-{[4-methyl-2-(trifluoromethyl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2-bromo-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-[(2-{3-azabicyclo[3.1.0]hexan-3-yl}-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; 1-[3-bromo-4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; 2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methylpropanamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclobutane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methylpyrimidin-5-yl]acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-hydroxyphenyl]acetamide; 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methyl]cyclopropane-1-carboxamide; N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-{[2-(azepan-1-yl)-4-methoxyphenyl](5-methylfuran-2-yl)methyl}-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]-2-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]acetamide; N-[(2-chloro-4-methylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; N-[(4-chloro-2-methylphenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; N-[(2,4-dichlorophenyl)(5-methylfuran-2-yl)methyl]-1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]cyclopropane-1-carboxamide; 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclobutane-1-carboxamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-2-methyl-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}propanamide; 1-[2-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-5-yl]-N-[(4-methoxy-2-methylphenyl)(5-methylfuran-2-yl)methyl]cyclopropane-1-carboxamide; 1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}cyclopropane-1-carboxamide; 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[3-methyl-1-[2-(piperidin-1-yl)phenyl]butyl]cyclopropane-1-carboxamide; 1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]-N-[(5-methylfuran-2-yl)[2-(piperidin-1-yl)phenyl]methyl]cyclopropane-1-carboxamide; 2-[4-(1,1-dioxo-1-thiomorpholin-4-yl)-3-hydroxyphenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(methoxymethyl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; 2-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-(hydroxymethyl)phenyl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; 2-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyrimidin-2-yl]-N-{[4-methyl-2-(piperidin-1-yl)phenyl](5-methylfuran-2-yl)methyl}acetamide; N-[(5-chlorofuran-2-yl)(2,4-dimethylphenyl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; N-[(5-chlorofuran-2-yl)(4-methylphenyl)methyl]-1-[4-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)phenyl]cyclopropane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[3-(1,1-dioxo-1-thiomorpholin-4-yl)-4-methoxyphenyl]cyclopropane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-2-methylphenyl]cyclopropane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-6-methylpyridin-2-yl]cyclopropane-1-carboxamide; N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)-3-methylpyridin-2-yl]cyclopropane-1-carboxamide; and N-[(2,4-dimethylphenyl)(5-methylfuran-2-yl)methyl]-1-[5-(1,1-dioxo-1-thiomorpholin-4-yl)pyridin-2-yl]cyclopropane-1-carboxamide.
 9. A combination product comprising: i) a compound of formula (Ia) as defined in claim 1, or a pharmaceutically acceptable salt thereof; and ii) another therapeutically active agent, such as a PPAR activator.
 10. The combination product according to claim 9, component ii) is Elafibranor, seladelpar, saroglitazar, lanifibranor, pioglitazone or a pharmaceutically acceptable salt thereof.
 11. The combination product according to claim 9, wherein the combination product is a composition comprising components i) and ii) and a pharmaceutically acceptable carrier.
 12. The combination product according to claim 9, wherein the combination product is a kit of parts comprising components i) and ii), for sequential, separate or simultaneous use.
 13. The combination product according to claim 9, wherein components i) and ii) are formulated in an injectable suspension, a gel, an oil, a pill, a tablet, a suppository, a powder, a capsule, an aerosol, an ointment, a cream, a patch, or means of galenic forms for a prolonged and/or slow release.
 14. (canceled)
 15. A method for the treatment of an autoimmune disease, an autoimmune-related disease, an inflammatory disease, a metabolic disease, a fibrotic disease or a cholestatic disease, wherein said method comprises administering to a subject in need thereof a therapeutically effective amount of a compound according to claim
 1. 16. A method for the treatment of an autoimmune disease, an autoimmune-related disease, an inflammatory disease, a metabolic disease, a fibrotic disease or a cholestatic disease, wherein said method comprises administering to a subject in need thereof a therapeutically effective amount of the combination product according to claim
 9. 